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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6607695/
https://www.ncbi.nlm.nih.gov/pubmed/31297131
http://dx.doi.org/10.3389/fgene.2019.00608

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6607695/
https://www.ncbi.nlm.nih.gov/pubmed/31297131
http://dx.doi.org/10.3389/fgene.2019.00608

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