A Novel Bi‐allelic Loss‐of‐Function Variant in...

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Clinical Genetics 2019 / 07

A Novel Bi‐allelic Loss‐of‐Function Variant in MYOD1 : Further evidence for gene‐disease association and phenotypic variability in MYOD1 related myopathy

Shukla, Anju, Narayanan, Dhanya Lakshmi, Asher, Urja, Girisha, Katta Mohan
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Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.13596
Date:
July, 2019
File:
PDF, 1.04 MB
english, 2019
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