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A third locus for dominant optic atrophy on chromosome 22q
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| Published in: | Journal of medical genetics 2005-01, Vol.42 (1), p.e1-e1 |
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| Main Authors: | , , , , , , , , , , |
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| Language: | English |
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| container_end_page | e1 |
| container_issue | 1 |
| container_start_page | e1 |
| container_title | Journal of medical genetics |
| container_volume | 42 |
| creator | Barbet, F Hakiki, S Orssaud, C Gerber, S Perrault, I Hanein, S Ducroq, D Dufier, J-L Munnich, A Kaplan, J Rozet, J-M |
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| doi_str_mv | 10.1136/jmg.2004.025502 |
| format | article |
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epidemiology</topic><topic>Electronic Letter</topic><topic>Family</topic><topic>Female</topic><topic>France - epidemiology</topic><topic>Genes</topic><topic>Genomes</topic><topic>Genotype & phenotype</topic><topic>GTP Phosphohydrolases - genetics</topic><topic>Haplotypes</topic><topic>Humans</topic><topic>Male</topic><topic>Mutation</topic><topic>Optic Atrophy, Autosomal Dominant - epidemiology</topic><topic>Optic Atrophy, Autosomal Dominant - genetics</topic><topic>Phenols</topic><topic>Prevalence</topic><topic>Visual acuity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barbet, F</creatorcontrib><creatorcontrib>Hakiki, S</creatorcontrib><creatorcontrib>Orssaud, C</creatorcontrib><creatorcontrib>Gerber, S</creatorcontrib><creatorcontrib>Perrault, I</creatorcontrib><creatorcontrib>Hanein, S</creatorcontrib><creatorcontrib>Ducroq, D</creatorcontrib><creatorcontrib>Dufier, J-L</creatorcontrib><creatorcontrib>Munnich, A</creatorcontrib><creatorcontrib>Kaplan, J</creatorcontrib><creatorcontrib>Rozet, J-M</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>ProQuest Biological Science Journals</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - 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| identifier | ISSN: 0022-2593 |
| ispartof | Journal of medical genetics, 2005-01, Vol.42 (1), p.e1-e1 |
| issn | 0022-2593 1468-6244 1468-6244 |
| language | eng |
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| source | PubMed Central |
| subjects | ADOA Atrophy autosomal dominant optic atrophy Chromosome Mapping Chromosomes Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 3 Denmark - epidemiology Electronic Letter Family Female France - epidemiology Genes Genomes Genotype & phenotype GTP Phosphohydrolases - genetics Haplotypes Humans Male Mutation Optic Atrophy, Autosomal Dominant - epidemiology Optic Atrophy, Autosomal Dominant - genetics Phenols Prevalence Visual acuity |
| title | A third locus for dominant optic atrophy on chromosome 22q |
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