Clinical exome sequencing identified a nonsense mutation in TMC1 gene causing profound hearing loss /
Alobathani, Maryam
Clinical exome sequencing identified a nonsense mutation in TMC1 gene causing profound hearing loss / by Maryam Alobathani ; supervised by Abdullah Al Mutery, Abdelaziz Tlili. - 2019. - 40 leaves : col. ill. ; 30 cm.+ 1 CD-Rom (4 3/4 in.)
A thesis submitted in partial fulfilment of the requirements for the degree of Master of Science in Biotechnology.
Thesis (M.Sc.)--University of Sharjah, 2019.
Bibligraphy: leaves 36-40.
Includes abstract in English.
Gift
University of Sharjah--Dissertations.
Deafness--genetics
Ear--abnormalities--United Arab Emirates.
Hearing Loss--etiology--United Arab Emirates.
Hearing Loss--genetics--United Arab Emirates.
WV270 / AL453c 2019
Clinical exome sequencing identified a nonsense mutation in TMC1 gene causing profound hearing loss / by Maryam Alobathani ; supervised by Abdullah Al Mutery, Abdelaziz Tlili. - 2019. - 40 leaves : col. ill. ; 30 cm.+ 1 CD-Rom (4 3/4 in.)
A thesis submitted in partial fulfilment of the requirements for the degree of Master of Science in Biotechnology.
Thesis (M.Sc.)--University of Sharjah, 2019.
Bibligraphy: leaves 36-40.
Includes abstract in English.
Gift
University of Sharjah--Dissertations.
Deafness--genetics
Ear--abnormalities--United Arab Emirates.
Hearing Loss--etiology--United Arab Emirates.
Hearing Loss--genetics--United Arab Emirates.
WV270 / AL453c 2019