Associated Papers
Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness.
Rayat S et al.
Bmc Medical Genomics, 2022
Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran.
Mohseni M et al.
Clinical Genetics, 2021
How Transmembrane Inner Ear (TMIE) plays role in the auditory system: A mystery to us.
Farhadi M et al.
Journal of Cellular and Molecular Medicine, 2021
The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations.
Yan D et al.
Genetic Testing and Molecular Biomarkers, 2015
Non-syndromic hearing impairment in India: high allelic heterogeneity among mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE.
Ganapathy A et al.
Plos One, 2014
High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays.
Kothiyal P et al.
Bmc Biotechnology, 2010
20146813 (PubMed )
Supplement: 1472-6750-10-10-S1.PDF
Select a paper to view details