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Truncating Variant in Myof Gene Is Associated With Limb-Girdle Type Muscular Dystrophy and Cardiomyopathy

Even though genetic studies of individuals with neuromuscular diseases have uncovered the molecular background of many cardiac disorders such as cardiomyopathies and inherited arrhythmic syndromes, the genetic cause of a proportion of cardiomyopathies associated with neuromuscular phenotype still re...

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Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Kiselev, Artem, Vaz, Raquel, Knyazeva, Anastasia, Sergushichev, Alexey, Dmitrieva, Renata, Khudiakov, Aleksandr, Jorholt, John, Smolina, Natalia, Sukhareva, Ksenia, Fomicheva, Yulia, Mikhaylov, Evgeny, Mitrofanova, Lubov, Predeus, Alexander, Sjoberg, Gunnar, Rudenko, Dmitriy, Sejersen, Thomas, Lindstrand, Anna, Kostareva, Anna
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6607695/
https://ncbi.nlm.nih.gov/pubmed/31297131
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2019.00608
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