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Mutations in TJP2, encoding zona occludens 2, and liver disease
Progressive familial intrahepatic cholestasis is a clinical description of a phenotype, which we now realize has several different genetic aetiologies. The identification of the underlying genetic defects has helped to elucidate important aspects of liver physiology. The latest addition to this fami...
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| Publicado no: | Tissue Barriers |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4574888/ https://ncbi.nlm.nih.gov/pubmed/26451340 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/21688370.2015.1026537 |
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