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New case of mitochondrial HMG-CoA synthase deficiency....

European Journal of Medical Genetics 2013 / 08 Vol. 56; Iss. 8

New case of mitochondrial HMG-CoA synthase deficiency. Functional analysis of eight mutations

Ramos, Mónica, Menao, Sebastián, Arnedo, María, Puisac, Beatriz, Gil-Rodríguez, María Concepción, Teresa-Rodrigo, María Esperanza, Hernández-Marcos, María, Pierre, Germaine, Ramaswami, Uma, Baquero-Mo
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Volume:
56
Language:
english
Journal:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2013.05.008
Date:
August, 2013
File:
PDF, 804 KB
english, 2013
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