Linkage analysis of DFNB3 locus causing hearing loss in human - Brossura

Ali, Akhtar; Babar, Masroor Ellahi

Brossura

ISBN 10: 3659377635 ISBN 13: 9783659377631

Casa editrice: LAP LAMBERT Academic Publishing, 2013

Riassunto

Deafness is a hearing impairment and can be classified as genetic or acquired, pre-lingual or post-lingual and syndromic or non-syndromic. This book contains details of materials, methods, literature,results and other information which will enable to study the linkage of genetic deafness. Consanguineous families of different ethnic groups having deaf individuals were studied. Pedigrees were drawn of all families having three or more affected members and showed recessive mode of inheritance. DNA was extracted from blood samples. Short Tandem Repeat markers for DFNB3 locus were amplified using PCR and genotyped for identification of hereditary hearing loss due to DFNB3 in Pakistani families.

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L'autore

Received Bachelor degree from IUB, Bahawalpur in Medicine & Surgery and completed one year internship at Hijaz Hospital, Gullberg III, Lahore. Then earned M.Phil in Molecular Biology & Biotechnology from UVAS, Lahore. Also doing Ph.D in the same discipline. Since postgraduation, engaged in various research projects at IBBT, UVAS, Lahore.

Dettagli dell'edizione

• Editore: LAP LAMBERT Academic Publishing
• Data di pubblicazione: 2013
• Lingua: Inglese
• ISBN 10: 3659377635
• ISBN 13: 9783659377631
• Rilegatura: Copertina flessibile
• Numero di pagine: 76
• Contatto del produttore: non disponibile
• Persona responsabile: KreGa Onlinehandel GmbH; 4950000000000; info@krega-onlinehandel.de; ; Birkenweg 31; Brakel; 33034; Germania