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• W337380068 abstract "Journal of Inherited Metabolic DiseaseVolume 20, Issue 3 p. 363-366 Article Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: Report on three novel mutations E176K, W409X and 1223 + 37 de199 V. Kožich, V. Kožich Institute of Inherited Metabolic Disorders, Charles University 1st Faculty of Medicine, Prague, Czech RepublicSearch for more papers by this authorM. Janošík, M. Janošík Institute of Inherited Metabolic Disorders, Charles University 1st Faculty of Medicine, Prague, Czech RepublicSearch for more papers by this authorJ. Sokolová, J. Sokolová Institute of Inherited Metabolic Disorders, Charles University 1st Faculty of Medicine, Prague, Czech RepublicSearch for more papers by this authorJ. Oliveriusová, J. Oliveriusová Institute of Inherited Metabolic Disorders, Charles University 1st Faculty of Medicine, Prague, Czech RepublicSearch for more papers by this authorM. Orendáč, M. Orendáč Institute of Inherited Metabolic Disorders, Charles University 1st Faculty of Medicine, Prague, Czech RepublicSearch for more papers by this authorJ. P. Kraus, J. P. Kraus Department of Pediatrics, University of Colorado School of Medicine, Denver, Colorado, USASearch for more papers by this authorD. Elleder, D. Elleder Institute of Inherited Metabolic Disorders, Charles University 1st Faculty of Medicine, Prague, Czech RepublicSearch for more papers by this author V. Kožich, V. Kožich Institute of Inherited Metabolic Disorders, Charles University 1st Faculty of Medicine, Prague, Czech RepublicSearch for more papers by this authorM. Janošík, M. Janošík Institute of Inherited Metabolic Disorders, Charles University 1st Faculty of Medicine, Prague, Czech RepublicSearch for more papers by this authorJ. Sokolová, J. Sokolová Institute of Inherited Metabolic Disorders, Charles University 1st Faculty of Medicine, Prague, Czech RepublicSearch for more papers by this authorJ. Oliveriusová, J. Oliveriusová Institute of Inherited Metabolic Disorders, Charles University 1st Faculty of Medicine, Prague, Czech RepublicSearch for more papers by this authorM. Orendáč, M. Orendáč Institute of Inherited Metabolic Disorders, Charles University 1st Faculty of Medicine, Prague, Czech RepublicSearch for more papers by this authorJ. P. Kraus, J. P. Kraus Department of Pediatrics, University of Colorado School of Medicine, Denver, Colorado, USASearch for more papers by this authorD. Elleder, D. Elleder Institute of Inherited Metabolic Disorders, Charles University 1st Faculty of Medicine, Prague, Czech RepublicSearch for more papers by this author First published: 01 July 1997 https://doi.org/10.1023/A:1005325911665Citations: 13AboutPDF 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 Volume20, Issue3July 1997Pages 363-366 RelatedInformation" @default.
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• W337380068 title "Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: Report on three novel mutations E176K, W409X and 1223 + 37 de199" @default.
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