Associated Papers
Research of genetic bases of hereditary non-syndromic hearing loss.
Subaşıoğlu A et al.
Turk Pediatri Arsivi, 2017
Identification of novel variants in the TMIE gene of patients with nonsyndromic hearing loss.
Yang JJ et al.
International Journal of Pediatric Otorhinolaryngology, 2010
A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia.
Sirmaci A et al.
Clinical Genetics, 2009
Novel sequence variants in the TMIE gene in families with autosomal recessive nonsyndromic hearing impairment.
Santos RL et al.
Journal of Molecular Medicine (berlin, Germany), 2006
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