Brief Report of Variants Detected in Hereditary Hearing Loss Cases in Iran over a 3-Year Period

• Main Authors: Niloofar BAZAZZADEGAN (Author), Raheleh VAZEHAN (Author), Mahsa FADAEE (Author), Zohreh FATTAHI (Author), Ayda ABOLHASSANI (Author), Elham PARSIMEHR (Author), Zahra KALHOR (Author), Mehrshid FARAJI ZONOOZ (Author), Fatemeh AHANGARI (Author), Shima DEHDAHSI (Author), Farshide SAMIEE (Author), Payman JAMALI (Author), Haleh HABIBI (Author), Younes NOURIZADEH (Author), Shokouh MAHDAVI (Author), Maryam BEHESHTIAN (Author), Ariana KARIMINEJAD (Author), Richard JH SMITH (Author), Hossein NAJMABADI (Author)
• Formato: Livro
• Publicado em: Tehran University of Medical Sciences, 2019-10-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: Connect to this object online.

Background: Diagnosis of hereditary hearing loss (HHL) as a heterogeneous disorder is very important espe-cially in countries with high rates of consanguinity where the autosomal recessive pattern of inheritance is preva-lent. Techniques such as next-generation sequencing, a comprehensive genetic te...