CLINICAL FEATURES AND DIAGNOSTIC ALGORITHMS OF CARDIOMYOPATHIES WITH RESTRICTIVE PHENOTYPE CAUSED BY CARDIAC TROPONIN I AND DESMIN GENES MUTATIONS

The authors are citing the literature data and share their own experiences of observation of two patients with cardiomyopathy associated with restrictive phenotype caused by mutations in defined genes encoding the synthesis of cardiac troponin I and desmin gene. Particular attention of the authors i...

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Bibliographic Details
Main Authors: M.V. Tural'chuk, G.A. Novik, A.Ya. Gudkova
Format: Article
Language:English
Published: Paediatrician Publishers, LLC 2011-08-01
Series:Pediatričeskaâ Farmakologiâ
Online Access:https://pf.spr-journal.ru/jour/article/view/1255