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

✍ Scribed by Robert Aquaron; Nadem Soufir; Jean-Louis Bergé-Lefranc; Catherine Badens; Frederic Austerlitz; Bernard Grandchamp

• Publisher: Nature Publishing Group
• Year: 2007
• Tongue: English
• Weight: 228 KB
• Volume: 52
• Category: Article
• ISSN: 1435-232X
• DOI: 10.1007/s10038-007-0181-y