17805552

Source:http://linkedlifedata.com/resource/pubmed/id/17805552

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0205314, umls-concept:C0270726, umls-concept:C0679622, umls-concept:C1184145, umls-concept:C1415042
pubmed:issue	5
pubmed:dateCreated	2007-10-3
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0412041
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Genetic Markers, http://linkedlifedata.com/resource/pubmed/chemical/Glial Fibrillary Acidic Protein
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0001-6322
pubmed:author	pubmed-author:HervaRiittaR, pubmed-author:HinttalaReettaR, pubmed-author:KarttunenAriA, pubmed-author:KarttunenVesaV, pubmed-author:RemesAnne MAM, pubmed-author:UusimaaJohannaJ
pubmed:issnType	Print
pubmed:volume	114
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	543-5
pubmed:meshHeading	pubmed-meshheading:17805552-Adult, pubmed-meshheading:17805552-Alexander Disease, pubmed-meshheading:17805552-Amino Acid Substitution, pubmed-meshheading:17805552-Astrocytes, pubmed-meshheading:17805552-Atrophy, pubmed-meshheading:17805552-Autopsy, pubmed-meshheading:17805552-Brain, pubmed-meshheading:17805552-DNA Mutational Analysis, pubmed-meshheading:17805552-Disease Progression, pubmed-meshheading:17805552-Fatal Outcome, pubmed-meshheading:17805552-Genetic Markers, pubmed-meshheading:17805552-Genetic Predisposition to Disease, pubmed-meshheading:17805552-Genotype, pubmed-meshheading:17805552-Glial Fibrillary Acidic Protein, pubmed-meshheading:17805552-Humans, pubmed-meshheading:17805552-Magnetic Resonance Imaging, pubmed-meshheading:17805552-Male, pubmed-meshheading:17805552-Muscular Atrophy, pubmed-meshheading:17805552-Mutation, pubmed-meshheading:17805552-Nerve Fibers, Myelinated, pubmed-meshheading:17805552-Occipital Lobe, pubmed-meshheading:17805552-Phenotype, pubmed-meshheading:17805552-Spinal Cord
pubmed:year	2007
pubmed:articleTitle	Alexander disease with occipital predominance and a novel c.799G>C mutation in the GFAP gene.
pubmed:publicationType	Letter, Case Reports, Research Support, Non-U.S. Gov't