Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.

Multiple deletions of mitochondrial DNA (mtDNA) have recently been reported in familial progressive external ophthalmoplegia (PEO), in a case of progressive encephalomyopathy, and in inherited recurrent myoglobinuria. The inheritance of familial PEO has been autosomal dominant, which indicates that...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Suomalainen, A, Majander, A, Haltia, M, Somer, H, Lönnqvist, J, Savontaus, M L, Peltonen, L
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1992
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC443063/
https://ncbi.nlm.nih.gov/pubmed/1634620
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