Identification of a founder mutation for Pendred syndrome...

Identification of a founder mutation for Pendred syndrome in families from northwest Iran

Mohseni, Marzieh, Honarpour, Asal, Mozafari, Reza, Davarnia, Behzad, Najmabadi, Hossein, Kahrizi, Kimia
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Volume:
78
Language:
english
Journal:
International Journal of Pediatric Otorhinolaryngology
DOI:
10.1016/j.ijporl.2014.08.035
Date:
November, 2014
File:
PDF, 1.38 MB
english, 2014
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