Ocular findings in patients with oculocutaneous albinism type ia with G47D tyrosinase gene mutation in Puerto Rico: a case report.

Rodr?guez-Agramonte F, Izquierdo NJ, Cadilla C. Ocular findings in patients with oculocutaneous albinism type ia with G47D tyrosinase gene mutation in Puerto Rico: a case report. Bol Asoc Med P R. 2013; 105(2):62-4.

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subject areas

Albinism, Oculocutaneous
Child
Child, Preschool
Humans
Male
Monophenol Monooxygenase
Mutation
Puerto Rico

authors with profiles

Carmen Cadilla

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