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Pulmonary artery pathologies in Alagille syndrome: a meta-analysis
Alagille syndrome, caused by mutations in the gene encoding Jagged1 (JAG1), a ligand in the Notch signaling pathway, is an autosomal dominant disorder with developmental abnormalities affecting the liver, heart, eyes, face and skeleton. The aim of the present study is try to disclose the clinical fe...
Autor principal: | Yuan, Shi-Min |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9421510/ https://www.ncbi.nlm.nih.gov/pubmed/36051836 http://dx.doi.org/10.5114/aic.2022.118526 |
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