GJB2-RELATED NON-SYNDROMIC HEARING LOSS VARIANTS’ SPECTRUM AND THEIR FREQUENCY IN TURKISH POPULATION

Objective: Hearing loss (HL) is one of the most prevalent chronic conditions in children and has consequences in speech, language, education, and social functioning which impede the quality of life. Due to the major involvement of the genetic factors in HL, especially non-syndromic HL (NSHL), geneti...

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Autors principals:	Çağrı Güleç, Ayça Dilruba Aslanger, Volkan Karaman, Bernd Wollnik, Fatih Tepgeç, Hülya Kayserili Karabey, Zehra Oya Uyguner
Format:	Artigo
Idioma:	Inglês
Publicat:	Istanbul University Press 2022-03-01
Col·lecció:	İstanbul Tıp Fakültesi Dergisi
Matèries:	sensorineural hearing loss gjb2 gene c.35delg alteration mutation frequency
Accés en línia:	https://cdn.istanbul.edu.tr/file/JTA6CLJ8T5/75CDC79D85D949E3AF3FFBA43E15B97D
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