Identification of a novel mutation in the paired domain of PAX3 in an Iranian family with Waardenburg syndrome Type I

Author: Sotirova Vihra N.   Rezaie Tayebeh   Khoshsorour M.R.   Sarfarazi Mansoor  

Publisher: Informa Healthcare

ISSN: 1381-6810

Source: Ophthalmic Genetics, Vol.21, Iss.1, 2000-03, pp. : 25-28

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