Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-2
pubmed:dateCreated
2001-11-9
pubmed:abstractText
We studied a 57-year-old female patient with clinical and biochemical evidences of McArdle's disease. Her muscle biopsy also revealed signs of mitochondrial proliferation, scattered RRF, and a deficit in complex I of the respiratory chain. Molecular genetic analysis showed that the patient was heterozygous for the most common mutation at codon 49 in the myophosphorylase gene. Mitochondrial DNA analysis of muscle tissue revealed an additional G-to-A transition at nucleotide position 7444 in the cytochrome c oxidase subunit I (COI) gene.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0022-510X
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
192
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
81-4
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:11701156-Codon, pubmed-meshheading:11701156-DNA, Mitochondrial, pubmed-meshheading:11701156-DNA Mutational Analysis, pubmed-meshheading:11701156-Electron Transport Complex I, pubmed-meshheading:11701156-Electron Transport Complex IV, pubmed-meshheading:11701156-Energy Metabolism, pubmed-meshheading:11701156-Exons, pubmed-meshheading:11701156-Female, pubmed-meshheading:11701156-Glycogen, pubmed-meshheading:11701156-Glycogen Phosphorylase, Muscle Form, pubmed-meshheading:11701156-Glycogen Storage Disease Type V, pubmed-meshheading:11701156-Humans, pubmed-meshheading:11701156-Middle Aged, pubmed-meshheading:11701156-Mitochondria, Muscle, pubmed-meshheading:11701156-Muscle, Skeletal, pubmed-meshheading:11701156-Muscle Fibers, Skeletal, pubmed-meshheading:11701156-NADH, NADPH Oxidoreductases, pubmed-meshheading:11701156-Point Mutation
pubmed:year
2001
pubmed:articleTitle
Mitochondrial DNA point mutation in the COI gene in a patient with McArdle's disease.
pubmed:affiliation
Servicios de Inmunología, Hospital Universitario Virgen del Rocío, Avda Manuel Siurot s/n, 41013 Seville, Spain. maguiler@cica.es
pubmed:publicationType
Journal Article, Case Reports, Research Support, Non-U.S. Gov't