Pathogenic Novel Heterozygous Variant c.1076c>T p. (Ser359Phe) chr1: 120512166 in NOTCH2 Gene, Type 2 Alagille Syndrome Causing Neonatal Cholestasis: A Case Report
Uddin, Mohammed Shahab, Al Fulayyih, Saleh, Al Denaini, Fatin Fahad, Al Hatlani, Maher Mohammed
Published in The American journal of case reports (06.10.2022)
Published in The American journal of case reports (06.10.2022)
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