A novel bi-allelic loss-of-function variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy MAHE Digital Repository

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 and Narayanan, Dhanya L and Asher, Urja and Girisha, KM (2019) A novel bi-allelic loss-of-function variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy. Clinical Genetics, 96 (3). pp. 276-277. ISSN 0009-9163

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Item Type:	Article
Subjects:	Medicine > KMC Manipal > Paediatrics
Depositing User:	KMC Library
Date Deposited:	17 Aug 2019 04:05
Last Modified:	17 Aug 2019 04:05
URI:	http://eprints.manipal.edu/id/eprint/154399

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