A Comprehensive Genetic and Clinical Evaluation of Waardenburg Syndrome Type II in a Set of Iranian Patients

Waardenburg syndrome (WS) is a neurocristopathy with an autosomal dominant mode of inheritance, and considerable clinical and genetic heterogeneity. WS type II is the most common type of WS in many populations presenting with sensorineural hearing impairment, heterochromia iridis, hypoplastic blue e...

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Publicat a:Int J Mol Cell Med
Autors principals: Jalilian, Nazanin, Tabatabaiefar, Mohammad Amin, Yazdanpanah, Mahboubeh, Darabi, Elham, Bahrami, Tayyeb, Zekri, Ali, Noori-Daloii, Mohammad Reza
Format: Artigo
Idioma:Inglês
Publicat: Babol University of Medical Sciences 2018
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Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6134422/
https://ncbi.nlm.nih.gov/pubmed/30234069
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.22088/IJMCM.BUMS.7.1.17
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