Author: "Meshkat, M" / Database: Gale General OneFile - Searchworks@Jio Institute Digital Library Search Results

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1. Identification of a novel GUCY2D mutation in an Iranian family with Leber Congenital Amaurosis

Author: Rezaie, T., Karimi-Nejad, M.H., Meshkat, M., Sohbati, S., Karimi-Nejad, R., Najmabadi, H., and Sarfarazi, M.
Subjects: Human genetics -- Research, Genetic disorders -- Research, Leber's congenital amaurosis -- Genetic aspects, Biological sciences
Published: 2001

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