A global view of the OCA2-HERC2 region and pigmentation

Mutations in the gene OCA2 are responsible for oculocutaneous albinism type 2, but polymorphisms in and around OCA2 have also been associated with normal pigment variation. In Europeans, three haplotypes in the region have been shown to be associated with eye pigmentation and a missense SNP (rs18004...

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Detalles Bibliográficos
Autores principales: Donnelly, Michael P., Paschou, Peristera, Grigorenko, Elena, Gurwitz, David, Barta, Csaba, Lu, Ru-Band, Zhukova, Olga V., Kim, Jong-Jin, Siniscalco, Marcello, New, Maria, Li, Hui, Kajuna, Sylvester L. B., Manolopoulos, Vangelis G., Speed, William C., Pakstis, Andrew J., Kidd, Judith R., Kidd, Kenneth K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3325407/
https://www.ncbi.nlm.nih.gov/pubmed/22065085
http://dx.doi.org/10.1007/s00439-011-1110-x

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