Literature DB >> 7465914

[Oculocutaneous albinism in Cameroun. About 216 cases (author's transl)].

R Aquaron.   

Abstract

Oculocutaneous albinism is a hereditary disease with a high incidence in Cameroon. The author has examined 216 cases. Most of them (70 per cent) are in Bamileke group where exist a great imbreeding tendency.

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Year:  1980        PMID： 7465914

Source DB:  PubMed          Journal:  Rev Epidemiol Sante Publique        ISSN： 0398-7620            Impact factor:   1.019


  1 in total

1.  Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P gene.

Authors:  Robert Aquaron; Nadem Soufir; Jean-Louis Bergé-Lefranc; Catherine Badens; Frederic Austerlitz; Bernard Grandchamp
Journal:  J Hum Genet       Date:  2007-09-01       Impact factor: 3.172
  1 in total

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