M13 - Mitochondrial disease and lipid storage myopathy due to mutation in CHCHD10 or DNM1L and disordered mitochondrial dynamics.

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Bibliographic Details
Title: M13 - Mitochondrial disease and lipid storage myopathy due to mutation in CHCHD10 or DNM1L and disordered mitochondrial dynamics.
Authors: Fratter, C., Dombi, E., Carver, J., Sergeant, K., Barbosa, I.A., Hofer, M., Esiri, M., Hilton-Jones, D., Jayawant, S., Olpin, S., Deshpande, C., Simpson, M.A., Poulton, J.
Source: Neuromuscular Disorders. Mar2017 Supplement 1, Vol. 27, pS21-S21. 1p.
Database: Academic Search Ultimate
Description
ISSN:09608966
DOI:10.1016/S0960-8966(17)30279-1