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Title:
Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12 | Human Genetics
Description:
The human gene encoding coproporphyrinogen oxidase is the defective gene in hereditary coproporphyria. This gene was mapped to chromosome band 3q12 using fluorescent in situ hybridization. The chromosomal localization was confirmed by cosegregation of the human gene with chromosome 3 in a panel of human/rodent somatic hybrids.
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human, google, scholar, article, gene, coproporphyrinogen, oxidase, privacy, cookies, genetics, chromosome, martasek, grandchamp, genet, content, publish, research, search, localization, bernard, situ, hybridization, access, hum, data, information, log, journal, band, cacheux, fougerousse, hereditary, coproporphyria, discover, nordmann, usa, download, france, springer, optional, analysis, personal, parties, policy, find, track, cite, valère, pavel, françoise,
Topics {✒️}
human/rodent somatic hybrids month download article/chapter chromosomal localization marie hélène delfau human coproporphyrinogen oxidase human chromosomes privacy choices/manage cookies chromosome band 3q12 human gene single-copy genes association claude bernard full article pdf delfau-larue mh metabolic basis european economic area common intragenic polymorphisms hôpital robert debr� faculté xavier bichat conditions privacy policy accepting optional cookies luc druart check access instant access main content log coproporphyrinogen oxidase defective gene journal finder publish article cacheux related subjects localization privacy policy personal data article log gene books a françoise fougerousse hereditary coproporphyria optional cookies article cite manage preferences pavel martasek subscription content data protection hum genet 81 hum genet 64 hum genet 94 essential cookies cookies skip bernard institution subscribe
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headline:Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12
description:The human gene encoding coproporphyrinogen oxidase is the defective gene in hereditary coproporphyria. This gene was mapped to chromosome band 3q12 using fluorescent in situ hybridization. The chromosomal localization was confirmed by cosegregation of the human gene with chromosome 3 in a panel of human/rodent somatic hybrids.
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Internal Medicine
Metabolic Disease
Human Gene
Chromosomal Localization
Gene Encode
Human Genetics
Molecular Medicine
Gene Function
Metabolic Diseases
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description:The human gene encoding coproporphyrinogen oxidase is the defective gene in hereditary coproporphyria. This gene was mapped to chromosome band 3q12 using fluorescent in situ hybridization. The chromosomal localization was confirmed by cosegregation of the human gene with chromosome 3 in a panel of human/rodent somatic hybrids.
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