THE MOUSE PINK-EYED DILUTION GENE - ASSOCIATION WITH HUMAN TYROSINASE-POSITIVE OCULOCUTANEOUS ALBINISM (OCA2), AND HYPOPIGMENTATION IN PRADER-WILLI-SYNDROME AND ANGELMAN SYNDROME
Mh. Brilliant et al., THE MOUSE PINK-EYED DILUTION GENE - ASSOCIATION WITH HUMAN TYROSINASE-POSITIVE OCULOCUTANEOUS ALBINISM (OCA2), AND HYPOPIGMENTATION IN PRADER-WILLI-SYNDROME AND ANGELMAN SYNDROME, American journal of human genetics, 53(3), 1993, pp. 161-161