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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Dettagli Bibliografici
Pubblicato in:Int J Mol Cell Med
Autori principali: Jalilian, Nazanin, Tabatabaiefar, Mohammad Amin, Yazdanpanah, Mahboubeh, Darabi, Elham, Bahrami, Tayyeb, Zekri, Ali, Noori-Daloii, Mohammad Reza
Natura: Artigo
Lingua:Inglês
Pubblicazione: Babol University of Medical Sciences 2018
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Original Article
Accesso online: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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