A novel 5-bp deletion in Clarin 1 in a family with Usher syndrome.

Autor: Akoury, Elie1 (AUTHOR), El Zir, Elie2 (AUTHOR), Mansour, Ahmad3 (AUTHOR), Mégarbané, André4 (AUTHOR), Majewski, Jacek5 (AUTHOR), Slim, Rima1 (AUTHOR) rima.slim@muhc.mcgill.ca
Zdroj: Ophthalmic Genetics. Dec2011, Vol. 32 Issue 4, p245-249. 5p.
Databáze: Academic Search Ultimate
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