Next Generation Sequencing approach to molecular diagnosis of Duchenne muscular dystrophy; identification of a novel mutation

Duchenne Muscular Dystrophy (DMD; MIM 310200) is one of the most common and severe type of hereditary muscular dystrophies. The disease is caused by mutations in the dystrophin gene. The dystrophin gene is associated with X-linked recessive Duchenne and Becker muscular dystrophy. This disease occurs...

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Veröffentlicht in:	Gene 2018-02, Vol.644, p.1-3
Hauptverfasser:	Ebrahimzadeh-Vesal, Reza, Teymoori, Atieh, Azimi-Nezhad, Mohsen, Hosseini, Forough Sadat
Format:	Artikel
Sprache:	eng
Schlagworte:	Duchenne muscular dystrophy Molecular diagnosis Next Generation Sequencing Novel mutation
Online-Zugang:	Volltext
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