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Methylmalonic aciduria cblB type: characterization of two novel mutations and mitochondrial dysfunction studies
Brasil, S., Richard, E., Jorge-Finnigan, A., Leal, F., Merinero, B., Banerjee, R., Desviat, L.R., Ugarte, M., Pérez, B.Volume:
87
Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.12426
Date:
June, 2015
File:
PDF, 742 KB
english, 2015