Mitochondrial DNA Haplogroups Do Not Play a Role in the Variable Phenotypic Presentation of the A3243G Mutation

Thirty-five mitochondrial (mt) DNAs from Spain that harbor the mutation A3243G in association with either MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes) syndrome or a wide array of disease phenotypes (ranging from diabetes and deafness to a mixture of chroni...

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Detalhes bibliográficos
Main Authors: Torroni, Antonio, Campos, Yolanda, Rengo, Chiara, Sellitto, Daniele, Achilli, Alessandro, Magri, Chiara, Semino, Ornella, García, Alberto, Jara, Pilar, Arenas, Joaquín, Scozzari, Rosaria
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society of Human Genetics 2003
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1180329/
https://ncbi.nlm.nih.gov/pubmed/12612863
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