Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred
| Autor: | Sadeghian, Ladan, Tabatabaiefar, Mohammad Amin, Fattahi, Najmeh, Pourreza, Mohammad Reza, Tahmasebi, Parisa, Alavi, Zahra, Hashemzadeh Chaleshtori, Morteza |
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| Zdroj: | In International Journal of Pediatric Otorhinolaryngology September 2019 124:99-105 |
| Databáze: | ScienceDirect |
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