AB032. Mutation spectrum in the dystrophin gene disclosed by multiplex ligation-dependent probe amplification in 181 Vietnamese Duchenne/Becker muscular dystrophy patients

Duchenne/Becker muscular dystrophy (DMD/BMD) the most common X-linked muscular dystrophy is caused by mutation in dystrophin gene. Deletion and duplication in the dystrophin gene account for 60-70% of mutation. Multiplex ligation-dependent probe amplification (MLPA) is the most powerful and convenie...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Ann Transl Med
Hlavní autoři: Tran, Van Khanh, Do, Ngoc Hai, Tran, Thinh Huy, Ta, Minh Hieu, Tuan-Pham, Le Anh, Chi, Dung Vu, Khanh, Nguyen Ngoc, Ta, Van Thanh, Matsuo, Masafumi
Médium: Artigo
Jazyk:Inglês
Vydáno: AME Publishing Company 2015
Témata:
Part 2: Symposium
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4563477/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB032
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky