Isolated mitochondrial myopathy due to m.3243A > G mutation in MT-TL1 gene

Acta Neurol Belg. 2022 Aug;122(4):1115-1116. doi: 10.1007/s13760-021-01598-1. Epub 2021 Jan 23.

Authors

Rohan R Mahale¹, Jyothi Gautham², Pooja Mailankody², Hansashree Padmanabha², P S Mathuranath²

Affiliations

¹ Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, 560029, India. [email protected].
² Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, 560029, India.

PMID: 33484420
DOI: 10.1007/s13760-021-01598-1

No abstract available

Keywords: MT-TL1 gene; Mitochondria; Myopathy; m.3243A > G.

Publication types

Letter

MeSH terms

DNA, Mitochondrial / genetics
Humans
MELAS Syndrome*
Mutation / genetics

Substances

DNA, Mitochondrial