Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patients.
Sign Up to like & getrecommendations! Published in 2017 at "International journal of pediatric otorhinolaryngology"
DOI: 10.1016/j.ijporl.2017.09.029
Abstract: Waardenburg syndrome (WS) is an auditory-pigmentary disease characterized by a clinical and genetic variability. WS is classified into four types depending on the presence or absence of additional symptoms: WS1, WS2, WS3 and WS4. Type… read more here.
Keywords: mutations causing; waardenburg syndrome; pax3 mutations; novel pax3 ... See more keywords