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

Anju Shukla; Dhanya L. Narayanan; Urja Asher; Katta M. Girisha

doi:10.1111/cge.13596

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

Anju Shukla, Dhanya L. Narayanan, Urja Asher, Katta M. Girisha

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	276-277
Number of pages	2
Journal	Clinical Genetics
Volume	96
Issue number	3
DOIs	https://doi.org/10.1111/cge.13596
Publication status	Published - 01-01-2019

All Science Journal Classification (ASJC) codes

Genetics
Genetics(clinical)

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10.1111/cge.13596

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title = "A novel bi-allelic loss-of-function variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy",

author = "Anju Shukla and Narayanan, {Dhanya L.} and Urja Asher and Girisha, {Katta M.}",

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AU - Asher, Urja

AU - Girisha, Katta M.

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

All Science Journal Classification (ASJC) codes

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