Cardiac Dysfunction in Duchenne Muscular Dystrophy Is Less Frequent in Patients With Mutations in the Dystrophin Dp116 Coding Region Than in Other Regions

BACKGROUND: Duchenne muscular dystrophy (DMD), the most common inherited muscular disease in childhood, is caused by dystrophin deficiency because of mutations in the DMD gene. Although DMD is characterized by fatal progressive muscle wasting, cardiomyopathy is the most important nonmuscle symptom t...

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Detalles Bibliográficos
Autores principales: Yamamoto, Tetsushi, Awano, Hiroyuki, Zhang, Zhujun, Sakuma, Mio, Kitaaki, Shoko, Matsumoto, Masaaki, Nagai, Masashi, Sato, Itsuko, Imanishi, Takamitsu, Hayashi, Nobuhide, Matsuo, Masafumi, Iijima, Kazumoto, Saegusa, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2018
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6319568/
https://www.ncbi.nlm.nih.gov/pubmed/29874176
http://dx.doi.org/10.1161/CIRCGEN.117.001782

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6319568/
https://www.ncbi.nlm.nih.gov/pubmed/29874176
http://dx.doi.org/10.1161/CIRCGEN.117.001782

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