학술논문
P115: Identification of a novel SDHB c.638T>G, p.M213R likely pathogenic variant accountable for hereditary paraganglioma-pheochromocytoma syndrome: A case report
Document Type
article
Author
Source
Genetics in Medicine Open, Vol 2, Iss , Pp 100996- (2024)
Subject
Language
English
ISSN
2949-7744