|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
3
|
|
pubmed:dateCreated |
2006-2-27
|
|
pubmed:abstractText |
Motor neuron disease (MND) is a common neurodegenerative condition for which the underlying cause is uncertain in many patients. We identified a patient with clinical features suggestive of MND but additional cardiac and metabolic symptoms. We wished to determine if the clinical features were due to a mitochondrial DNA mutation.
|
|
pubmed:grant |
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Mar
|
|
pubmed:issn |
0364-5134
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
59
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
570-4
|
|
pubmed:dateRevised |
2011-1-5
|
|
pubmed:meshHeading |
pubmed-meshheading:16358336-Aged,
pubmed-meshheading:16358336-DNA, Mitochondrial,
pubmed-meshheading:16358336-DNA Mutational Analysis,
pubmed-meshheading:16358336-Electron Transport Complex IV,
pubmed-meshheading:16358336-Humans,
pubmed-meshheading:16358336-Immunohistochemistry,
pubmed-meshheading:16358336-Male,
pubmed-meshheading:16358336-Motor Neuron Disease,
pubmed-meshheading:16358336-Motor Neurons,
pubmed-meshheading:16358336-Mutation,
pubmed-meshheading:16358336-RNA, Messenger,
pubmed-meshheading:16358336-RNA, Transfer, Ile,
pubmed-meshheading:16358336-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:16358336-Succinate Dehydrogenase
|
|
pubmed:year |
2006
|
|
pubmed:articleTitle |
Motor neuron disease in a patient with a mitochondrial tRNAIle mutation.
|
|
pubmed:affiliation |
Mitochondrial Research Group, School of Neurology, Neurobiology and Psychiatry, The Medical School, University of Newcastle upon Tyne, UK.
|
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Case Reports,
Research Support, Non-U.S. Gov't
|
