Ontology highlight
ABSTRACT:
SUBMITTER: Torroni A
PROVIDER: S-EPMC1180329 | biostudies-literature | 2003 Apr
REPOSITORIES: biostudies-literature
Torroni Antonio A Campos Yolanda Y Rengo Chiara C Sellitto Daniele D Achilli Alessandro A Magri Chiara C Semino Ornella O García Alberto A Jara Pilar P Arenas Joaquín J Scozzari Rosaria R
American journal of human genetics 20030224 4
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 chronic progressive external ophthalmoplegic symptoms and strokelike episodes) were studied by use of high-resolution restriction fragment length polymorphism analysis and control-region sequencing. A total ...[more]