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Two novel VPS33B mutations in a patient with arthrogryposis, renal dysfunction and cholestasis syndrome in mainland China

Arthrogryposis, renal dysfunction and cholestasis (ARC) syndrome is a rare genetic disorder and has not been described in China. We present a female infant with neonatal intrahepatic cholestasis from a Chinese family with ARC syndrome. All 23 coding exons and flanking introns of the VPS33B gene were...

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Detalhes bibliográficos
Main Authors: Li, Li-Ting, Zhao, Jing, Chen, Rui, Wang, Jian-She
Formato: Artigo
Idioma:Inglês
Publicado em: Baishideng Publishing Group Co., Limited 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3886028/
https://ncbi.nlm.nih.gov/pubmed/24415890
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v20.i1.326
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