Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene region.

Autor: Bergen, Arthur A.B., Brink, Jacoline B.ten, Riemslag, Frans, Schuurman, Ellen J.M., Tijmes, Nel
Zdroj: Human Molecular Genetics; May1995, Vol. 4 Issue 5, p931-935, 5p
Databáze: Complementary Index