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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Detalhes bibliográficos
Publicado no:Ann Transl Med
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: AME Publishing Company 2017
Assuntos:
Molecular Genetics, Genomics, Mechanisms of Diseases
Acesso em linha: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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