Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2001-10-10
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1468-6244
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
38
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
703-5
pubmed:dateRevised
2008-11-20
pubmed:meshHeading
pubmed-meshheading:11594340-Adult, pubmed-meshheading:11594340-Base Sequence, pubmed-meshheading:11594340-Cell Survival, pubmed-meshheading:11594340-Cells, Cultured, pubmed-meshheading:11594340-DNA Mutational Analysis, pubmed-meshheading:11594340-Electron Transport, pubmed-meshheading:11594340-Female, pubmed-meshheading:11594340-Fibroblasts, pubmed-meshheading:11594340-Genotype, pubmed-meshheading:11594340-Humans, pubmed-meshheading:11594340-Male, pubmed-meshheading:11594340-Middle Aged, pubmed-meshheading:11594340-Mitochondria, Muscle, pubmed-meshheading:11594340-Muscles, pubmed-meshheading:11594340-Mutation, pubmed-meshheading:11594340-Nucleic Acid Conformation, pubmed-meshheading:11594340-Ophthalmoplegia, Chronic Progressive External, pubmed-meshheading:11594340-Oxygen, pubmed-meshheading:11594340-Oxygen Consumption, pubmed-meshheading:11594340-Phenotype, pubmed-meshheading:11594340-RNA, pubmed-meshheading:11594340-RNA, Transfer, Tyr
pubmed:year
2001
pubmed:articleTitle
Functional characterisation of mitochondrial tRNA(Tyr) mutation (5877-->GA) associated with familial chronic progressive external ophthalmoplegia.
pubmed:publicationType
Letter, Research Support, Non-U.S. Gov't