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Molecular-Clinical Correlation in a Family With a Novel Heteroplasmic Leigh Syndrome Missense Mutation in the Mitochondrial Cytochrome c Oxidase III Gene
Mkaouar-Rebai, E., Ellouze, E., Chamkha, I., Kammoun, F., Triki, C., Fakhfakh, F.Volume:
26
Language:
english
Journal:
Journal of Child Neurology
DOI:
10.1177/0883073810371227
Date:
January, 2011
File:
PDF, 463 KB
english, 2011