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Author: personID (integer) : 950141
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Phenotypic variability and identification of novel YARS2 mutations in YARS2 mitochondrial myopathy, lactic acidosis and sideroblastic anaemia.

Lisa Riley , Minal Menezes , Joëlle Rudinger-Thirion , Rachael Duff , Pascale de Lonlay , et al.
Orphanet Journal of Rare Diseases, 2013, 8 (1), pp.193. ⟨10.1186/1750-1172-8-193⟩
Journal articles inserm-00921182v1
Image document

Phenotypic variability and identification of novel YARS2 mutations in YARS2 mitochondrial myopathy, lactic acidosis and sideroblastic anaemia.

Lisa Riley , Minal Menezes , Joëlle Rudinger-Thirion , Rachael Duff , Pascale de Lonlay , et al.
Orphanet Journal of Rare Diseases, 2013, 8 (1), pp.193. ⟨10.1186/1750-1172-8-193⟩
Journal articles inserm-00921185v1