Matches in SemOpenAlex for { <https://semopenalex.org/work/W2334721897> ?p ?o ?g. }
Showing items 1 to 69 of
69
with 100 items per page.
- W2334721897 endingPage "530" @default.
- W2334721897 startingPage "527" @default.
- W2334721897 abstract "Journal of Inherited Metabolic DiseaseVolume 16, Issue 3 p. 527-530 Short Communication Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD, Wolfram syndrome) A. Rötig, A. Rötig Unité de Recherches sur les Handicaps Génétiques de l'Enfant and Département de Pédiatrie, Hôpital des Enfants Malades, 149 Rue de Sèvres, Paris Cedex 15, 75743 FranceSearch for more papers by this authorV. Cormier, V. Cormier Unité de Recherches sur les Handicaps Génétiques de l'Enfant and Département de Pédiatrie, Hôpital des Enfants Malades, 149 Rue de Sèvres, Paris Cedex 15, 75743 FranceSearch for more papers by this authorP. Chatelain, P. Chatelain Service d'Endocrinologie et Diabétologie Pédiatrique, Hôpital Edouard Herriot, Place d'Arsonval, Lyon Cedex 03, 69437 FranceSearch for more papers by this authorR. Francois, R. Francois Service d'Endocrinologie et Diabétologie Pédiatrique, Hôpital Edouard Herriot, Place d'Arsonval, Lyon Cedex 03, 69437 FranceSearch for more papers by this authorJ. -M. Saudubray, J. -M. Saudubray Unité de Recherches sur les Handicaps Génétiques de l'Enfant and Département de Pédiatrie, Hôpital des Enfants Malades, 149 Rue de Sèvres, Paris Cedex 15, 75743 FranceSearch for more papers by this authorP. Rustin, P. Rustin Unité de Recherches sur les Handicaps Génétiques de l'Enfant and Département de Pédiatrie, Hôpital des Enfants Malades, 149 Rue de Sèvres, Paris Cedex 15, 75743 FranceSearch for more papers by this authorA. Munnich, A. Munnich Unité de Recherches sur les Handicaps Génétiques de l'Enfant and Département de Pédiatrie, Hôpital des Enfants Malades, 149 Rue de Sèvres, Paris Cedex 15, 75743 FranceSearch for more papers by this author A. Rötig, A. Rötig Unité de Recherches sur les Handicaps Génétiques de l'Enfant and Département de Pédiatrie, Hôpital des Enfants Malades, 149 Rue de Sèvres, Paris Cedex 15, 75743 FranceSearch for more papers by this authorV. Cormier, V. Cormier Unité de Recherches sur les Handicaps Génétiques de l'Enfant and Département de Pédiatrie, Hôpital des Enfants Malades, 149 Rue de Sèvres, Paris Cedex 15, 75743 FranceSearch for more papers by this authorP. Chatelain, P. Chatelain Service d'Endocrinologie et Diabétologie Pédiatrique, Hôpital Edouard Herriot, Place d'Arsonval, Lyon Cedex 03, 69437 FranceSearch for more papers by this authorR. Francois, R. Francois Service d'Endocrinologie et Diabétologie Pédiatrique, Hôpital Edouard Herriot, Place d'Arsonval, Lyon Cedex 03, 69437 FranceSearch for more papers by this authorJ. -M. Saudubray, J. -M. Saudubray Unité de Recherches sur les Handicaps Génétiques de l'Enfant and Département de Pédiatrie, Hôpital des Enfants Malades, 149 Rue de Sèvres, Paris Cedex 15, 75743 FranceSearch for more papers by this authorP. Rustin, P. Rustin Unité de Recherches sur les Handicaps Génétiques de l'Enfant and Département de Pédiatrie, Hôpital des Enfants Malades, 149 Rue de Sèvres, Paris Cedex 15, 75743 FranceSearch for more papers by this authorA. Munnich, A. Munnich Unité de Recherches sur les Handicaps Génétiques de l'Enfant and Département de Pédiatrie, Hôpital des Enfants Malades, 149 Rue de Sèvres, Paris Cedex 15, 75743 FranceSearch for more papers by this author First published: 01 May 1993 https://doi.org/10.1007/BF00711672Citations: 20AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Citing Literature Volume16, Issue3May 1993Pages 527-530 RelatedInformation" @default.
- W2334721897 created "2016-06-24" @default.
- W2334721897 creator A5005829538 @default.
- W2334721897 creator A5023844947 @default.
- W2334721897 creator A5029002217 @default.
- W2334721897 creator A5042925067 @default.
- W2334721897 creator A5062746059 @default.
- W2334721897 creator A5065034733 @default.
- W2334721897 creator A5079413672 @default.
- W2334721897 date "1993-05-01" @default.
- W2334721897 modified "2023-09-30" @default.
- W2334721897 title "Deletion of mitochondrial DNA in a case of early‐onset diabetes mellitus, optic atrophy and deafness (DIDMOAD, Wolfram syndrome)" @default.
- W2334721897 cites W1978341753 @default.
- W2334721897 cites W2002933566 @default.
- W2334721897 cites W2014394445 @default.
- W2334721897 cites W2019039833 @default.
- W2334721897 cites W2160604203 @default.
- W2334721897 doi "https://doi.org/10.1007/bf00711672" @default.
- W2334721897 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/7609443" @default.
- W2334721897 hasPublicationYear "1993" @default.
- W2334721897 type Work @default.
- W2334721897 sameAs 2334721897 @default.
- W2334721897 citedByCount "24" @default.
- W2334721897 countsByYear W23347218972012 @default.
- W2334721897 countsByYear W23347218972013 @default.
- W2334721897 countsByYear W23347218972014 @default.
- W2334721897 countsByYear W23347218972015 @default.
- W2334721897 crossrefType "journal-article" @default.
- W2334721897 hasAuthorship W2334721897A5005829538 @default.
- W2334721897 hasAuthorship W2334721897A5023844947 @default.
- W2334721897 hasAuthorship W2334721897A5029002217 @default.
- W2334721897 hasAuthorship W2334721897A5042925067 @default.
- W2334721897 hasAuthorship W2334721897A5062746059 @default.
- W2334721897 hasAuthorship W2334721897A5065034733 @default.
- W2334721897 hasAuthorship W2334721897A5079413672 @default.
- W2334721897 hasConcept C134018914 @default.
- W2334721897 hasConcept C138885662 @default.
- W2334721897 hasConcept C15708023 @default.
- W2334721897 hasConcept C187212893 @default.
- W2334721897 hasConcept C555293320 @default.
- W2334721897 hasConcept C71924100 @default.
- W2334721897 hasConceptScore W2334721897C134018914 @default.
- W2334721897 hasConceptScore W2334721897C138885662 @default.
- W2334721897 hasConceptScore W2334721897C15708023 @default.
- W2334721897 hasConceptScore W2334721897C187212893 @default.
- W2334721897 hasConceptScore W2334721897C555293320 @default.
- W2334721897 hasConceptScore W2334721897C71924100 @default.
- W2334721897 hasIssue "3" @default.
- W2334721897 hasLocation W23347218971 @default.
- W2334721897 hasLocation W23347218972 @default.
- W2334721897 hasOpenAccess W2334721897 @default.
- W2334721897 hasPrimaryLocation W23347218971 @default.
- W2334721897 hasRelatedWork W1563850031 @default.
- W2334721897 hasRelatedWork W1995515455 @default.
- W2334721897 hasRelatedWork W2011278875 @default.
- W2334721897 hasRelatedWork W2411973762 @default.
- W2334721897 hasRelatedWork W2415759662 @default.
- W2334721897 hasRelatedWork W2748952813 @default.
- W2334721897 hasRelatedWork W2899084033 @default.
- W2334721897 hasRelatedWork W3031052312 @default.
- W2334721897 hasRelatedWork W3032375762 @default.
- W2334721897 hasRelatedWork W3036934084 @default.
- W2334721897 hasVolume "16" @default.
- W2334721897 isParatext "false" @default.
- W2334721897 isRetracted "false" @default.
- W2334721897 magId "2334721897" @default.
- W2334721897 workType "article" @default.