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^*

^*Corresponding author for this work

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

7 Citations (Scopus)

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

Cite this

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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.\}",

year = "2019",

month = jan,

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doi = "10.1111/cge.13596",

language = "English",

volume = "96",

pages = "276--277",

journal = "Clinical Genetics",

issn = "0009-9163",

publisher = "Wiley-Blackwell Publishing Ltd",

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TY - JOUR

T1 - A novel bi-allelic loss-of-function variant in MYOD1

T2 - Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy

AU - Shukla, Anju

AU - Narayanan, Dhanya L.

AU - Asher, Urja

AU - Girisha, Katta M.

PY - 2019/1/1

Y1 - 2019/1/1

UR - https://www.scopus.com/pages/publications/85068762620

UR - https://www.scopus.com/pages/publications/85068762620#tab=citedBy

U2 - 10.1111/cge.13596

DO - 10.1111/cge.13596

M3 - Letter

C2 - 31260566

AN - SCOPUS:85068762620

SN - 0009-9163

VL - 96

SP - 276

EP - 277

JO - Clinical Genetics

JF - Clinical Genetics

IS - 3

ER -

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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