Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes

BACKGROUND: Congenital dilatation of the bile-duct (CDD) is a rare, mostly sporadic, disorder that results in bile retention with severe associated complications. CDD affects mainly Asians. To our knowledge, no genetic study has ever been conducted. METHODS: We aim to identify genetic risk factors b...

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Библиографические подробности
Опубликовано в: :BMC Med Genomics
Главные авторы: Wong, John K. L., Campbell, Desmond, Ngo, Ngoc Diem, Yeung, Fanny, Cheng, Guo, Tang, Clara S. M., Chung, Patrick H. Y., Tran, Ngoc Son, So, Man-ting, Cherny, Stacey S., Sham, Pak C., Tam, Paul K., Garcia-Barcelo, Maria-Mercè
Формат: Artigo
Язык:Inglês
Опубликовано: BioMed Central 2016
Предметы:
Research Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC5154011/
https://ncbi.nlm.nih.gov/pubmed/27955658
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-016-0236-z
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