P467: A novel mutation in HSPG2 gene causing Schwartz Jampel syndrome

P467: A novel mutation in HSPG2 gene causing Schwartz Jampel syndrome

Bibliographic Details
Main Author:	Parminder Parminder
Format:	Article
Language:	English
Published:	Elsevier 2024-01-01
Series:	Genetics in Medicine Open
Online Access:	http://www.sciencedirect.com/science/article/pii/S2949774424005077

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