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Reversible mitochondrial myopathy with cytochrome c oxidase deficiency.

Two siblings, a boy and a girl born in a nonconsanguineous marriage, presented with a similar clinical course. Sucking and breathing difficulties appeared within a few weeks of birth. Clinical examination revealed profound muscular hypotonia, hepatomegaly, increased serum creatine kinase activities,...

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Detalhes bibliográficos
Main Authors: Salo, M K, Rapola, J, Somer, H, Pihko, H, Koivikko, M, Tritschler, H J, DiMauro, S
Formato: Artigo
Idioma:Inglês
Publicado em: 1992
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1793596/
https://ncbi.nlm.nih.gov/pubmed/1325759
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