A MYH3 mutation was identified for the first time in a...

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Neuromuscular Disorders 2018 / 3

A MYH3 mutation was identified for the first time in a chinese family with sheldon-hall syndrome (DA2B)

Xu, Yang, Kang, Qing-Lin, Zhang, Zhen-Lin
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Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2018.03.002
Date:
March, 2018
File:
PDF, 1.05 MB
english, 2018
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