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
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- Material Type
- 記事
- Author/Editor
- Robert AquaronNadem SoufirJean-Louis Berge-Lefranc 他
- Author Heading
- Periodical title
- Journal of human genetics / Japan Society of Human Genetics
- No. or year of volume/issue
- 52(9) 2007
- Volume
- 52
- Issue
- 9
- Pages
- 771～780
- Publication date of volume/issue (W3CDTF)
- 2007