Open AccessLow Heteroplasmy Rates Argue Against the m.3243A>G Variant as the Cause of Auditory Agnosia
Author(s) -
Josef Finsterer
Publication year - 2020
Publication title -
the neurologist/the neurologist
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.43
H-Index - 60
eISSN - 2331-2637
pISSN - 1074-7931
DOI - 10.1097/nrl.0000000000000247
Subject(s) - heteroplasmy , medicine , mitochondrial encephalomyopathy , lactic acidosis , epilepsy , pediatrics , stroke (engine) , audiology , psychiatry , mutation , mechanical engineering , biochemistry , chemistry , engineering , gene