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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Front Genet
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Frontiers Media S.A. 2019
Gaiak:
Genetics
Sarrera elektronikoa: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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