Novel insights into the genetic profile of hereditary spastic paraplegia in India-Reference-Cited by-同舟云学术

Novel insights into the genetic profile of hereditary spastic paraplegia in India

Published:2022-01-02 Issue:1 Volume:36 Page:21-31
ISSN:0167-7063
Container-title:Journal of Neurogenetics
language:en
Short-container-title:Journal of Neurogenetics

Author:

Narendiran Sundarapandian¹,Debnath Monojit²,Shivaram Sumanth¹,Kannan Ramakrishnan³^ORCID,Sharma Shivani¹,Christopher Rita⁴,Seshagiri Doniparthi V.¹,Jain Sanjeev³,Purushottam Meera³^ORCID,Mangalore Sandhya⁵,Bharath Rose Dawn⁵,Bindu Parayil Sankaran⁵,Sinha Sanjib⁵,Taly Arun B.¹,Nagappa Madhu¹^ORCID

Affiliation:

1. Departments of Neurology and Human Genetics, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India

2. Department of Psychiatry, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India

3. Department of Neurochemistry, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India

4. Department of Neuroimaging and Interventional Radiology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India

5. National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India

Publisher

Informa UK Limited

Subject

Cellular and Molecular Neuroscience,Genetics

Link

https://www.tandfonline.com/doi/pdf/10.1080/01677063.2022.2064463

Reference50 articles.

1. Oculomotor apraxia and disrupted sleep with nocturnal ballistic bouts in ADCY5-related disease

2. VAMP1 Mutation Causes Dominant Hereditary Spastic Ataxia in Newfoundland Families

3. Clinical and genetic study of hereditary spastic paraplegia in Canada

4. Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study

5. Child Neurology: Spastic paraparesis and dystonia with a novel ADCY5 mutation

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