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Pathological evaluation of rats carrying in-frame mutations in the dystrophin gene: a new model of Becker muscular dystrophy

Dystrophin, encoded by the DMD gene on the X chromosome, stabilizes the sarcolemma by linking the actin cytoskeleton with the dystrophin-glycoprotein complex (DGC). In-frame mutations in DMD cause a milder form of X-linked muscular dystrophy, called Becker muscular dystrophy (BMD), characterized by...

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Detalles Bibliográficos
Autores principales:	Teramoto, Naomi, Sugihara, Hidetoshi, Yamanouchi, Keitaro, Nakamura, Katsuyuki, Kimura, Koichi, Okano, Tomoko, Shiga, Takanori, Shirakawa, Taku, Matsuo, Masafumi, Nagata, Tetsuya, Daimon, Masao, Matsuwaki, Takashi, Nishihara, Masugi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Company of Biologists Ltd 2020
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541341/ https://www.ncbi.nlm.nih.gov/pubmed/32859695 http://dx.doi.org/10.1242/dmm.044701

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