Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis?

Jouanolle, A M; Fergelot, P; Raoul, M L; Gandon, G; Roussey, M; Deugnier, Y; Feingold, J; Le Gall, J Y; David, V

Jouanolle, A M; Fergelot, P; Raoul, M L; Gandon, G; Roussey, M; Deugnier, Y; Feingold, J; Le Gall, J Y; David, V.

Affiliation

Jouanolle AM; Service de Génétique Moléculaire et Hormonologie, CHU Pontchaillou, Rennes, France.

Ann Genet ; 41(4): 195-8, 1998.

Article in En | MEDLINE | ID: mdl-9881181

Subject(s)

Hemochromatosis/epidemiology; Hemochromatosis/genetics; Membrane Proteins; Penetrance; Alleles; Cohort Studies; DNA Mutational Analysis; France/epidemiology; Gene Frequency; Genes, MHC Class I; Genetic Carrier Screening; HLA Antigens/genetics; Hemochromatosis Protein; Histocompatibility Antigens Class I/genetics; Homozygote; Humans; Infant, Newborn; Prevalence

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Collection: 01-internacional Database: MEDLINE Main subject: Penetrance / Hemochromatosis / Membrane Proteins Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limits: Humans / Newborn Country/Region as subject: Europa Language: En Journal: Ann Genet Year: 1998 Document type: Article Affiliation country: France Country of publication: Netherlands

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