Connexin 26 gene in non-syndromic hearing loss /
Mona Ahmed Elakkad
Connexin 26 gene in non-syndromic hearing loss / ضعف السمع الغير متلازم و الجين كونكسين ٢٦ Mona Ahmed Elakkad ; Supervised Ahmad Sameh Farid , Mohamed Ibrahim Shabana , Maha Hassan AbouElew - Cairo : Mona Ahmed Elakkad , 2012 - 111 P. : charts ; 25cm
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
Connexin 26 GJB2 Nonsyndromic autosomal recessive sensorineural hearing loss
Connexin 26 gene in non-syndromic hearing loss / ضعف السمع الغير متلازم و الجين كونكسين ٢٦ Mona Ahmed Elakkad ; Supervised Ahmad Sameh Farid , Mohamed Ibrahim Shabana , Maha Hassan AbouElew - Cairo : Mona Ahmed Elakkad , 2012 - 111 P. : charts ; 25cm
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
Connexin 26 GJB2 Nonsyndromic autosomal recessive sensorineural hearing loss