- Tytuł:
- Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China.
- Autorzy:
- Źródło:
- Acta oto-laryngologica [Acta Otolaryngol] 2013 Sep; Vol. 133 (9), pp. 930-4. Date of Electronic Publication: 2013 Jul 09.
- Typ publikacji:
- Journal Article; Research Support, Non-U.S. Gov't
- MeSH Terms:
-
Connexins/*genetics
Membrane Transport Proteins/*genetics
RNA, Ribosomal/*genetics
Adolescent ; Adult ; Aged ; Child ; Child, Preschool ; Connexin 26 ; Deafness/epidemiology ; Deafness/ethnology ; Deafness/genetics ; Female ; Humans ; Male ; Middle Aged ; Mongolia/epidemiology ; Mongolia/ethnology ; Mutation ; Polymorphism, Genetic ; Sulfate Transporters ; Tibet/epidemiology ; Tibet/ethnology ; Young Adult - SCR Disease Name:
- Nonsyndromic Deafness
Czasopismo naukowe