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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Detaylı Bibliyografya
Asıl Yazarlar: Torroni, Antonio, Campos, Yolanda, Rengo, Chiara, Sellitto, Daniele, Achilli, Alessandro, Magri, Chiara, Semino, Ornella, García, Alberto, Jara, Pilar, Arenas, Joaquín, Scozzari, Rosaria
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The American Society of Human Genetics 2003
Konular:
Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1180329/
https://ncbi.nlm.nih.gov/pubmed/12612863
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