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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2003-7-4
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pubmed:abstractText |
To report mutations in the OPA1 gene in Japanese patients with bilateral optic atrophy unassociated with mitochondrial DNA mutations at nt 11778, 3460, and 14484.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
0021-5155
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pubmed:author |
pubmed-author:Budu,
pubmed-author:EndoMachiM,
pubmed-author:EsaTenriT,
pubmed-author:FujikiKeikoK,
pubmed-author:HayasakaSeijiS,
pubmed-author:HayasakaYorikoY,
pubmed-author:KanaiAtsushiA,
pubmed-author:MatsumotoMasayukiM,
pubmed-author:MurakamiAkiraA,
pubmed-author:NagakiYasunoriY,
pubmed-author:YamadaTetsuyaT
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pubmed:issnType |
Print
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pubmed:volume |
47
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
409-11
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:12842213-Adolescent,
pubmed-meshheading:12842213-Adult,
pubmed-meshheading:12842213-Child,
pubmed-meshheading:12842213-Child, Preschool,
pubmed-meshheading:12842213-DNA, Mitochondrial,
pubmed-meshheading:12842213-DNA Mutational Analysis,
pubmed-meshheading:12842213-Female,
pubmed-meshheading:12842213-GTP Phosphohydrolases,
pubmed-meshheading:12842213-Genotype,
pubmed-meshheading:12842213-Humans,
pubmed-meshheading:12842213-Japan,
pubmed-meshheading:12842213-Male,
pubmed-meshheading:12842213-Middle Aged,
pubmed-meshheading:12842213-Mitochondria,
pubmed-meshheading:12842213-Mutation, Missense,
pubmed-meshheading:12842213-Optic Atrophy,
pubmed-meshheading:12842213-Polymerase Chain Reaction
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pubmed:articleTitle |
OPA1 gene mutations in Japanese patients with bilateral optic atrophy unassociated with mitochondrial DNA mutations at nt 11778, 3460, and 14484.
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pubmed:affiliation |
Department of Ophthalmology, Toyama Medical and Pharmaceutical University, Toyama, Japan.
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pubmed:publicationType |
Journal Article
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