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A novel ABCB11 mutation in an Iranian girl with progressive familial intrahepatic cholestasis
Progressive familial intrahepatic cholestasis is an autosomal recessive liver disorder caused by (biallelic) mutations in the ATP8B1 of ABCB11 gene. A nine-year-old girl with cholestasis was referred for genetic counseling. She had a family history of cholestasis in two previous expired siblings. Ge...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3841569/ https://ncbi.nlm.nih.gov/pubmed/24339557 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.120813 |
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