AB095. Prenatal diagnosis of Duchenne muscular dystrophy by combining of multiplex Polymerase Chain Reaction and Multiplex Ligation dependent Probe Amplification

BACKGROUND: Duchenne muscular dystrophy (DMD) is the most common allelic X-linked muscular disorder caused by mutation in the dystrophin gene. The dystrophin gene located at Xp21.2, is one of the largest known human genes, covering 2.2 Mb, containing 79 exons and at least eight independent, tissue s...

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Dades bibliogràfiques
Publicat a:Ann Transl Med
Autors principals: Ngo, Manh Tien, Nguyen, Thi Phuong Mai, Ngo, Thi Tuyet Nhung, Nguyen, Thi Mai Huong, An, Thuy Lan, Ngo, Diem Ngoc, Vu, Chi Dung, Bui, Phuong Thao
Format: Artigo
Idioma:Inglês
Publicat: AME Publishing Company 2017
Matèries:
Molecular Genetics, Genomics, Mechanisms of Diseases
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5641754/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2017.s095
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