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

Author: Aquaron Robert   Soufir Nadem   Bergé-Lefranc Jean-Louis   Badens Catherine   Austerlitz Frederic   Grandchamp Bernard  

Publisher: Springer Publishing Company

ISSN: 1434-5161

Source: Journal of Human Genetics, Vol.52, Iss.9, 2007-09, pp. : 771-780

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