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pro vyhledávání: '"Dániel M. Péter"'
Autor:
Dalma Kellermayer, Hedvig Tordai, Balázs Kiss, György Török, Dániel M. Péter, Alex Ali Sayour, Miklós Pólos, István Hartyánszky, Bálint Szilveszter, Siegfried Labeit, Ambrus Gángó, Gábor Bedics, Csaba Bödör, Tamás Radovits, Béla Merkely, Miklós S.Z. Kellermayer
Heterozygous (HET) truncating mutations in the TTN gene (TTNtv) encoding the giant titin protein are the most common genetic cause of dilated cardiomyopathy (DCM). However, the molecular mechanisms by which TTNtv mutations induce DCM are controversia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0149ccb0fcb1c8874689c6a1c5ef3f7
https://doi.org/10.1101/2023.02.08.527678
https://doi.org/10.1101/2023.02.08.527678
