What can we learn from the Distribution of the 2.7kb Deletion Mutation of the OCA2 Gene in Oculocutaneous Albinism Type 2 (OCA2) in Cameroon and in Sub-Saharan Countries?
The specific African intragenic deletion of the 2.7-kb of the OCA2 gene was determined in a 408 OCA2 patients from Cameroon with an allele frequency of 0.68, a value close to that found in other... View HTML Download PDF
Robert Aquaron*, Jean-Louis Berge-Lefranc, Eulalie Lassaux, Claudio Plaisant, Benoit Arveiler and Murray Brilliant