11
Jul
Alagille syndrome and deletion 20p12
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Alagille Syndrome and deletion 20p12 Alagille syndrome is an autosomal dominant disorder that affects several bodily systems resulting in liver, cardiac, ocular, skeletal, vascular, and renal abnormalities. Alagille syndrome is usually (95%) caused by malfunction of the JAG1 gene located on the short arm of chromosome 20 (20p12 region). Although... Read More
