Randomly amplified polymorphic dna (RAPD) and connexin-26 gene sequence analysis of non-syndromic heredofamilial hearing loss (Record no. 50756)

MARC details
000 -LEADER
fixed length control field 02671cab a2200277Ia 45 0
001 - CONTROL NUMBER
control field u197835
003 - CONTROL NUMBER IDENTIFIER
control field SIRSI
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 110906s2007 ua ss b eng d
040 ## - CATALOGING SOURCE
Original cataloging agency EAL
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) ART EJGC V36 No2 2
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Saad, M. M.
240 10 - UNIFORM TITLE
Uniform title Egyptian journal of genetics and cytology, 2007. v. 36 (2)
Medium [electronic resource].
245 10 - TITLE STATEMENT
Title Randomly amplified polymorphic dna (RAPD) and connexin-26 gene sequence analysis of non-syndromic heredofamilial hearing loss
Medium [electronic resource].
300 ## - PHYSICAL DESCRIPTION
Extent p.219-225.
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note Includes references.
520 ## - SUMMARY, ETC.
Summary, etc. Hearing loss is a multifactorial disorder resulting from both genetic and environmental factors. About 90 to 100 genes were identified for non-syndromic heredofamilial sensorineural hearing loss. Among different known genes, Connexin-26 gene mutations are reported to be re-sponsible for half of all hereditary hearing loss in many countries. A single known mutation, 35 delG, is the most common mutation in Connexin-26 gene. The pre-sent study aimed to identify the patterns resulting from Randomly Amplified Polymorphic DNA (RAPD) analysis, to search for specific band(s) that character-ize genes affecting hearing, and to detect mutations in Connexin-26 gene resulting in heredofamilial hearing loss. DNA isolation was carried out for fifteen patients and seven healthy rela-tives and subjected to RAPD-PCR analysis. Eleven patients were subjected to Connexin-26 gene sequencing. Gene se-quencing of Connexin-26 reveals muta-tion in only one patient, which, suggests that mutations other than Connexin-26 genes may be implicated in non-syn-dromic heredofamilial hearing loss in Upper Egypt. The dendrogram, that fol-lowed RAPD analysis, classified patients into three groups, suggesting the presence of three possible mutations responsible for this type of hearing loss. Complete analysis of the obtained bands revealed that band 485 bp is the only one existing in all examined patients and relatives, while the other 35 bands are polymorphic. Some bands (965, 950, 730 and 80 bp) are absent in all seven relatives, but present in some of the affected patients. These bands can be used as diagnostic bands, as their presence can identify patients with non-syndromic heredofamilial hearing loss.
596 ## -
-- 1
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Deafness, Noise induced.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Hearing levels.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Connexins.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Mohamad, N. A.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Mohamad, G. I. A.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Mohamad, H. A.
773 0# - HOST ITEM ENTRY
Title Egyptian Journal of Genetics and Cytology.
Related parts 2007.v.36(2)
International Standard Serial Number 0046-161X
Control subfield nnas
Record control number u197829
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="http://nile.enal.sci.eg/EALE/2007/EJGC/3607/2/219.pdf">http://nile.enal.sci.eg/EALE/2007/EJGC/3607/2/219.pdf</a>
Public note Full Text Article.
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Articles
Source of classification or shelving scheme Library of Congress Classification

No items available.


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