Connexin 26 gene in non-syndromic hearing loss / Mona Ahmed Elakkad ; Supervised Ahmad Sameh Farid , Mohamed Ibrahim Shabana , Maha Hassan AbouElew
Material type:
- ضعف السمع الغير متلازم و الجين كونكسين ٢٦ [Added title page title]
- Issued also as CD
Item type | Current library | Home library | Call number | Copy number | Status | Barcode | |
---|---|---|---|---|---|---|---|
![]() |
قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.12.Ph.D.2012.Mo.C (Browse shelf(Opens below)) | Not for loan | 01010110059622000 | ||
![]() |
مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.12.Ph.D.2012.Mo.C (Browse shelf(Opens below)) | 59622.CD | Not for loan | 01020110059622000 |
Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of E.N.T
Mutations in GJB2 gene, encoding the gap-junction protein connexion 26 (Cx26) are the leading cause of deafness in autosomal recessive nonsyndromic sensorineural hearing loss (ARNSHL) and the 35delG mutation is the most common in many ethnic groups. To evaluate the extent of contribution of the 35delG mutation of GJB2 gene to ARNSHL in the Egyptian population as well as to correlate the clinical relevance of this mutation to the severity of hearing loss HL
Issued also as CD
There are no comments on this title.