Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India-Reference-Cited by-同舟云学术

Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India

Published:2016-03 Issue: Volume:27 Page:1-5
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Bindu Parayil Sankaran,Govindaraju Chikanna,Sonam Kothari,Nagappa Madhu,Chiplunkar Shwetha,Kumar Rakesh,Gayathri Narayanappa,Bharath MM Srinivas,Arvinda Hanumanthapura R.,Sinha Sanjib,Khan Nahid Akthar,Govindaraj Periyasamy,Nunia Vandana,Paramasivam Arumugam,Thangaraj Kumarasamy,Taly Arun B.

Funder

of Biotechnology, Govt of India

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

Reference38 articles.

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4. Variable phenotype including leigh syndrome with a 9185T>C mutation in the MTATP6 gene;Childs;Neuropediatrics,2007

5. SURF1 deficiency causes demyelinating Charcot–Marie–Tooth disease;Echaniz-Laguna;Neurology,2013

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