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Defective mitochondrial ATPase due to rare mtDNA m.8969G>A mutation – Causing poor growth, developmental delay and lactic acidosis
Isohanni, P., Carroll, C., Suomalainen, A., Lönnqvist, T.Volume:
21
Language:
english
Journal:
European Journal of Paediatric Neurology
DOI:
10.1016/j.ejpn.2017.04.1045
Date:
June, 2017
File:
PDF, 59 KB
english, 2017