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Revista De Neurologia|June 18, 2004
[Familiar chronic progressive external ophthalmoplegia of mitochondrial origin]M Pineda, A Playán-Ariso, M J Alcaine-Villarroya, et al.
Orphanet Journal of Rare Diseases|February 1, 2018
Hypermanganesemia due to mutations in SLC39A14: further insights into Mn deposition in the central nervous systemL Marti-Sanchez, J D Ortigoza-Escobar, A Darling, et al.
Clinical Genetics|March 19, 2010
Molecular characterization of five patients with homocystinuria due to severe methylenetetrahydrofolate reductase deficiencyR Urreizti, A A Moya-García, A Pino-Ángeles, et al.
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