Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Mutations: The First Report from South Asia and Comprehensive Literature Review-Reference-Cited by-同舟云学术

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Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Mutations: The First Report from South Asia and Comprehensive Literature Review

Published:2021 Issue:3 Volume:17 Page:409
ISSN:1738-6586
Container-title:Journal of Clinical Neurology
language:en
Short-container-title:J Clin Neurol

Author:

Polavarapu Kiran¹²^ORCID,Bardhan Mainak¹^ORCID,Anjanappa Ram Murthy³^ORCID,Vengalil Seena¹^ORCID,Preethish-Kumar Veeramani¹^ORCID,Shingavi Leena¹^ORCID,Chawla Tanushree¹,Nashi Saraswati¹^ORCID,Mohan Dhaarini¹,Arunachal Gautham³,Geetha Thenral S.⁴,Ramprasad Vedam⁴,Nalini Atchayaram¹^ORCID

Affiliation:

1. Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.

2. Children's Hospital of Eastern Ontario Research Institute; Division of Neurology, Department of Medicine, The Ottawa Hospital; Brain and Mind Research Institute, University of Ottawa, Ottawa, ON, Canada.

3. Department of Human Genetics, National Institute of Mental Health and Neurosciences, Bengaluru, India.

4. Medgenome, Medgenome Labs, Bommasandra, Bangalore, India.

Publisher

Korean Neurological Association

Subject

Clinical Neurology,Neurology

Link

https://thejcn.com/pdf/10.3988/jcn.2021.17.3.409

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