Establishment of a human induced pluripotent stem cell line from a patient with Alagille syndrome carrying heterozygous mutation in JAG1 gene
Alagille syndrome (ALGS) is a complex rare genetic disorder that involves multiple organ systems. We established an induced pluripotent stem cell (iPSC) line from peripheral blood mononuclear cells of a one-year-old boy with Alagille syndrome carrying a heterozygous mutation c.234C > A (p.C78X) i...
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| Auteurs principaux: | , |
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| Format: | Article |
| Langue: | anglais |
| Publié: |
Elsevier
2025-09-01
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| Collection: | Stem Cell Research |
| Accès en ligne: | http://www.sciencedirect.com/science/article/pii/S1873506125001382 |
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