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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
Robert Aquaron, Nadem Soufir, Jean-Louis Bergé-Lefranc, Catherine Badens, Frederic Austerlitz, Bernard GrandchampVolume:
52
Language:
english
Pages:
10
DOI:
10.1007/s10038-007-0181-y
Date:
September, 2007
File:
PDF, 228 KB
english, 2007