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Connexin 26 gene in non-syndromic hearing loss / Mona Ahmed Elakkad ; Supervised Ahmad Sameh Farid , Mohamed Ibrahim Shabana , Maha Hassan AbouElew

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Mona Ahmed Elakkad , 2012Description: 111 P. : charts ; 25cmOther title:
  • ضعف السمع الغير متلازم و الجين كونكسين ٢٦ [Added title page title]
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Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of E.N.T Summary: 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
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Item type Current library Home library Call number Copy number Status Barcode
Thesis Thesis 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
CD - Rom CD - Rom 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

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