학술논문
Mutations in PTPN11 could lead to a congenital myasthenic syndrome phenotype: a Noonan syndrome case series
Document Type
Article
Author
Source
In: Journal of Neurology . (Journal of Neurology, March 2024, 271(3):1331-1341)
Subject
Language
English
ISSN
14321459
03405354
03405354