Rare variant in LAMA2 gene causing congenital muscular dystrophy in a Sudanese family. A case report

Congenital muscular dystrophies (CMD) are a heterogeneous group of disorders caused by mutations in musculoskeletal proteins. The most common type of CMD in Europe is Merosin-deficient CMD caused by mutations in laminin-α2 protein. Very few studies reported pathogenic variants underlying these disor...

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Библиографические подробности
Опубликовано в: :Acta Myol
Главные авторы: AMIN, MUTAZ, BAKHIT, YOUSUF, KOKO, MAHMOUD, IBRAHIM, MOHAMED OSAMA MIRGAHNI, SALIH, MA, IBRAHIM, MUNTASER, SEIDI, OSHEIK A
Формат: Artigo
Язык:Inglês
Опубликовано: Pacini Editore srl 2019
Предметы:
Case Reports
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC6598405/
https://ncbi.nlm.nih.gov/pubmed/31309178
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