학술논문
Paternal uniparental disomy of chromosome 2 resulting in a concurrent presentation of Crigler–Najjar syndrome type I and long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Document Type
Article
Author
Source
In: American Journal of Medical Genetics, Part A . (American Journal of Medical Genetics, Part A, June 2022, 188(6):1848-1852)
Subject
Language
English
ISSN
15524833
15524825
15524825