Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

Autor:	Gerald V. Raymond, Haggit Hurvitz, Gert Matthijs, Barbara Schenk, Markus Aebi, Jaak Jaeken, Christian Frank, Isabelle Korn-Lubetzki, Annick Raas-Rotschild, Timo Imbach, T Hennet, Anthony Luder, Claudia E. Grubenmann, Eric G. Berger, Shoshana Revel-Vik
Rok vydání:	2003
Předmět:	Genetics business.industry Clinical investigation medicine General Medicine Corrigendum medicine.disease business Congenital disorder of glycosylation
Zdroj:	Journal of Clinical Investigation. 111:209-216
ISSN:	0021-9738
DOI:	10.1172/jci200316336
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac756b48395aa4d84f4aa8526d233dc5 https://doi.org/10.1172/jci200316336 Zobrazit plný text záznamu