Whole‐exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations-Reference-Cited by-同舟云学术

Whole‐exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations

Published:2020-11-26 Issue:3 Volume:28 Page:992-1003
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Sanga Shamita¹^ORCID,Ghosh Arnab¹,Kumar Krishna²,Polavarapu Kiran³,Preethish‐Kumar Veeramani³^ORCID,Vengalil Seena³,Nashi Saraswati³,Bardhan Mainak³^ORCID,Arunachal Gautham⁴,Raju Sanita³,Gayathri Narayanappa⁵,Biswas Nidhan K.¹,Chakrabarti Saikat²,Nalini Atchayaram³^ORCID,Roy Sudipto⁶⁷⁸,Acharya Moulinath¹^ORCID

Affiliation:

1. National Institute of Biomedical Genomics Kalyani India

2. Structural Biology and Bioinformatics Division Indian Institute of Chemical Biology Kolkata India

3. Department of Neurology National Institute of Mental Health and Neuroscience Bengaluru India

4. Department of Human Genetics National Institute of Mental Health and Neuroscience Bengaluru India

5. Department of Neuropathology National Institute of Mental Health and Neuroscience Bengaluru India

6. Institute of Molecular and Cell Biology Singapore City Singapore

7. Department of Biological Sciences National University of Singapore Singapore City Singapore

8. Department of Pediatrics Yong Loo Lin School of Medicine National University of Singapore Singapore City Singapore

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ene.14616

Reference51 articles.

1. Congenital muscular dystrophies: New aspects of an expanding group of disorders

2. Muscular dystrophies: An Indian scenario

3. Approach to the diagnosis of congenital myopathies

4. Congenital myopathies: Natural history of a large pediatric cohort

5. Congenital Muscular Dystrophies: A Brief Review

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