This shareable PDF can be hosted on any platform or network and is fully compliant with publisher copyright.
A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family
- Asma Behlouli, Crystel Bonnet, Samia Abdi, Mokhtar Hasbellaoui, Farid Boudjenah, Jean-Pierre Hardelin, Malek Louha, Mohamed Makrelouf, Fatima Ammar-Khodja, Akila Zenati, Christine Petit
- International Journal of Pediatric Otorhinolaryngology, August 2016, Elsevier
- DOI: 10.1016/j.ijporl.2016.04.040