Mitochondrial dysfunction in human skeletal muscle biopsies of lipid storage disorder-Reference-Cited by-同舟云学术

Mitochondrial dysfunction in human skeletal muscle biopsies of lipid storage disorder

Published:2018-04-19 Issue:4 Volume:145 Page:323-341
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:J. Neurochem.

Author:

Debashree Bandopadhyay¹,Kumar Manish²³,Keshava Prasad Thottethodi Subrahmanya²⁴,Natarajan Archana¹,Christopher Rita¹,Nalini Atchayaram⁵,Bindu Parayil Sankaran⁵,Gayathri Narayanappa⁶,Srinivas Bharath Muchukunte Mukunda¹^ORCID

Affiliation:

1. Department of Neurochemistry; National Institute of Mental Health and Neurosciences (NIMHANS); Bangalore India

2. Institute of Bioinformatics; Bangalore Karnataka India

3. Manipal University; Manipal Karnataka India

4. Center for Systems Biology and Molecular Medicine; Yenepoya University; Mangalore Karnataka India

5. Department of Neurology; National Institute of Mental Health and Neurosciences (NIMHANS); Bangalore India

6. Department of Neuropathology; National Institute of Mental Health and Neurosciences (NIMHANS); Bangalore India

Funder

Indian Council of Medical Research

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jnc.14318/fullpdf

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5. Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosis;Aral;Am. J. Hum. Genet.,1997

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