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• W2038344265 abstract "Journal of Inherited Metabolic DiseaseVolume 6, Issue S2 p. 95-96 Short Communication Multiple molybdoenzyme deficiencies due to an inborn error of molybdenum cofactor metabolism: Two additional cases in a new family A. Munnich, A. Munnich Clinique et Unité de Recherches de Génétique Médicale (INSERM U-12), Hôpital des Enfants-Malades, Paris, Cedex 15, 75743 FranceSearch for more papers by this authorJ. M. Saudubray, J. M. Saudubray Clinique et Unité de Recherches de Génétique Médicale (INSERM U-12), Hôpital des Enfants-Malades, Paris, Cedex 15, 75743 FranceSearch for more papers by this authorC. Charpentier, C. Charpentier Clinique et Unité de Recherches de Génétique Médicale (INSERM U-12), Hôpital des Enfants-Malades, Paris, Cedex 15, 75743 FranceSearch for more papers by this authorH. Ogier, H. Ogier Clinique et Unité de Recherches de Génétique Médicale (INSERM U-12), Hôpital des Enfants-Malades, Paris, Cedex 15, 75743 FranceSearch for more papers by this authorF. X. Coudé, F. X. Coudé Clinique et Unité de Recherches de Génétique Médicale (INSERM U-12), Hôpital des Enfants-Malades, Paris, Cedex 15, 75743 FranceSearch for more papers by this authorJ. Frézal, J. Frézal Clinique et Unité de Recherches de Génétique Médicale (INSERM U-12), Hôpital des Enfants-Malades, Paris, Cedex 15, 75743 FranceSearch for more papers by this authorL. Yacoub, L. Yacoub Hôpital Universitaire, Sousse, TunisieSearch for more papers by this authorA. Harbi, A. Harbi Hôpital Universitaire, Sousse, TunisieSearch for more papers by this authorS. Snoussi, S. Snoussi Hôpital Universitaire, Sousse, TunisieSearch for more papers by this author A. Munnich, A. Munnich Clinique et Unité de Recherches de Génétique Médicale (INSERM U-12), Hôpital des Enfants-Malades, Paris, Cedex 15, 75743 FranceSearch for more papers by this authorJ. M. Saudubray, J. M. Saudubray Clinique et Unité de Recherches de Génétique Médicale (INSERM U-12), Hôpital des Enfants-Malades, Paris, Cedex 15, 75743 FranceSearch for more papers by this authorC. Charpentier, C. Charpentier Clinique et Unité de Recherches de Génétique Médicale (INSERM U-12), Hôpital des Enfants-Malades, Paris, Cedex 15, 75743 FranceSearch for more papers by this authorH. Ogier, H. Ogier Clinique et Unité de Recherches de Génétique Médicale (INSERM U-12), Hôpital des Enfants-Malades, Paris, Cedex 15, 75743 FranceSearch for more papers by this authorF. X. Coudé, F. X. Coudé Clinique et Unité de Recherches de Génétique Médicale (INSERM U-12), Hôpital des Enfants-Malades, Paris, Cedex 15, 75743 FranceSearch for more papers by this authorJ. Frézal, J. Frézal Clinique et Unité de Recherches de Génétique Médicale (INSERM U-12), Hôpital des Enfants-Malades, Paris, Cedex 15, 75743 FranceSearch for more papers by this authorL. Yacoub, L. Yacoub Hôpital Universitaire, Sousse, TunisieSearch for more papers by this authorA. Harbi, A. Harbi Hôpital Universitaire, Sousse, TunisieSearch for more papers by this authorS. Snoussi, S. Snoussi Hôpital Universitaire, Sousse, TunisieSearch for more papers by this author First published: 01 June 1983 https://doi.org/10.1007/BF01810344Citations: 14AboutPDF 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 Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article.Citing Literature Volume6, IssueS2June 1983Pages 95-96 RelatedInformation" @default.
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• W2038344265 title "Multiple molybdoenzyme deficiencies due to an inborn error of molybdenum cofactor metabolism: Two additional cases in a new family" @default.
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