LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation

Autosomal dominant LGMD1D has been described in multiple families in Asia, Europe, and USA. However, to the best of our knowledge, no cases of LGMD1D have been reported among native Bedouin Saudi families. Fifty Saudi families with LGMD were analyzed and the causative underlying genes were studied u...

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Detalles Bibliográficos
Autores principales: BOHLEGA, SAEED A., ALFAWAZ, SARAH, ABOU-AL-SHAAR, HUSSAM, AL-HINDI, HINDI N., MURAD, HATEM N., BOHLEGA, MOHAMED S., MEYER, BRIAN F., MONIES, DOROTA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pacini Editore srl 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390114/
https://www.ncbi.nlm.nih.gov/pubmed/30838352

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390114/
https://www.ncbi.nlm.nih.gov/pubmed/30838352

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