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Outcomes of Childhood Cholestasis in Alagille Syndrome: Results of a Multicenter Observational Study
Alagille syndrome (ALGS) is an autosomal dominant multisystem disorder with cholestasis as a defining clinical feature. We sought to characterize hepatic outcomes in a molecularly defined cohort of children with ALGS‐related cholestasis. Two hundred and ninety‐three participants with ALGS with nativ...
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| Publicado en: | Hepatol Commun |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7049675/ https://ncbi.nlm.nih.gov/pubmed/33313463 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hep4.1468 |
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