학술논문
MIRAGE Syndrome Caused by a De Novo c.3406G>C (p. Glu1136Gln) Mutation in the SAMD9 Gene Presenting With Neonatal Adrenal Insufficiency and Recurrent Intussusception: A Case Report.
Document Type
Article
Author
Source
Frontiers in Endocrinology; 9/29/2021, Vol. 12, p1-7, 7p
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Language
ISSN
16642392
Abstract
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