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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Detalhes bibliográficos
Publicado no:Int J Mol Cell Med
Main Authors: Jalilian, Nazanin, Tabatabaiefar, Mohammad Amin, Yazdanpanah, Mahboubeh, Darabi, Elham, Bahrami, Tayyeb, Zekri, Ali, Noori-Daloii, Mohammad Reza
Formato: Artigo
Idioma:Inglês
Publicado em: Babol University of Medical Sciences 2018
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Original Article
Acesso em linha: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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