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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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Publicado no: | BMC Med Genomics |
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Main Authors: | , , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
BioMed Central
2016
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Assuntos: | |
Acesso em linha: | 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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