Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1993-6-24
pubmed:abstractText
We report a patient with necrotizing encephalomyelopathy (Leigh's syndrome) associated with a deficiency of pyruvate dehydrogenase complex activity. The underlying mutation is an A to C transversion in the pyruvate dehydrogenase complex E1 alpha subunit gene. As the E1 alpha subunit is encoded on the X chromosome, this observation confirms that some patients with Leigh's syndrome may potentially exhibit X-linked inheritance.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0364-5134
pubmed:author
pubmed:issnType
Print
pubmed:volume
33
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
652-5
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:8498846-Amino Acid Sequence, pubmed-meshheading:8498846-Aspartic Acid, pubmed-meshheading:8498846-Base Sequence, pubmed-meshheading:8498846-Brain Stem, pubmed-meshheading:8498846-Cells, Cultured, pubmed-meshheading:8498846-Cesarean Section, pubmed-meshheading:8498846-Citrate (si)-Synthase, pubmed-meshheading:8498846-DNA, pubmed-meshheading:8498846-Exons, pubmed-meshheading:8498846-Fibroblasts, pubmed-meshheading:8498846-Gestational Age, pubmed-meshheading:8498846-Humans, pubmed-meshheading:8498846-Infant, Newborn, pubmed-meshheading:8498846-Leigh Disease, pubmed-meshheading:8498846-Leukocytes, pubmed-meshheading:8498846-Male, pubmed-meshheading:8498846-Mitochondria, Heart, pubmed-meshheading:8498846-Mitochondria, Liver, pubmed-meshheading:8498846-Molecular Sequence Data, pubmed-meshheading:8498846-Necrosis, pubmed-meshheading:8498846-Oligodeoxyribonucleotides, pubmed-meshheading:8498846-Point Mutation, pubmed-meshheading:8498846-Pyruvate Dehydrogenase Complex, pubmed-meshheading:8498846-Skin, pubmed-meshheading:8498846-X Chromosome
pubmed:year
1993
pubmed:articleTitle
Molecular genetic characterization of an X-linked form of Leigh's syndrome.
pubmed:affiliation
Department of Biochemistry, University of Oxford, UK.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Case Reports, Research Support, Non-U.S. Gov't