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Gene Therapy for Progressive Familial Intrahepatic Cholestasis: Current Progress and Future Prospects
Progressive Familial Intrahepatic Cholestasis (PFIC) are inherited severe liver disorders presenting early in life, with high serum bile salt and bilirubin levels. Six types have been reported, two of these are caused by deficiency of an ABC transporter; ABCB11 (bile salt export pump) in type 2; ABC...
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| Publicado no: | Int J Mol Sci |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7796371/ https://ncbi.nlm.nih.gov/pubmed/33383947 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22010273 |
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