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

Author:

Polavarapu Kiran12ORCID,Bardhan Mainak1ORCID,Anjanappa Ram Murthy3ORCID,Vengalil Seena1ORCID,Preethish-Kumar Veeramani1ORCID,Shingavi Leena1ORCID,Chawla Tanushree1,Nashi Saraswati1ORCID,Mohan Dhaarini1,Arunachal Gautham3,Geetha Thenral S.4,Ramprasad Vedam4,Nalini Atchayaram1ORCID

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

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