Otoferlin Gene Mutation in Non Syndromic Auditory Neuropathy patients
Ghada Moharram Mohamed Khalil;
Abstract
Identification of the underlying gene(s) for AN is one of the key challenges for understanding the molecular basis for different AN phenotypes. The genetic study of auditory neuropathy is complicated by the fact that the term includes hearing losses with
Other data
| Title | Otoferlin Gene Mutation in Non Syndromic Auditory Neuropathy patients | Other Titles | الاختلال الوراثي في جين أوتوفيرلين في مرض الاعتلال العصبي السمعي الغير مرتبط بمتلازمة | Authors | Ghada Moharram Mohamed Khalil | Keywords | Otoferlin Gene Mutation in Non Syndromic Auditory Neuropathy patients | Issue Date | 2010 | Description | Identification of the underlying gene(s) for AN is one of the key challenges for understanding the molecular basis for different AN phenotypes. The genetic study of auditory neuropathy is complicated by the fact that the term includes hearing losses with |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| Binder1.pdf | 631.17 kB | Adobe PDF | View/Open |
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