Alobathani, Maryam <br/><br/>
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.) 
<br/><br/> A thesis submitted in partial fulfilment of the requirements for the degree of Master of Science in Biotechnology. 
<br/><br/>Thesis (M.Sc.)--University of Sharjah, 2019. 
<br/><br/>Bibligraphy: leaves 36-40. 
<br/><br/><br/>Includes abstract in English. 
<br/><br/><label>Source: </label> Gift 
<br/><br/><label>Subjects--Corporate Names: </label><br/>University of Sharjah--Dissertations.
<br/><br/><label>Subjects--Topical Terms: </label><br/>Deafness--genetics <br/>Ear--abnormalities--United Arab Emirates.<br/>Hearing Loss--etiology--United Arab Emirates.<br/>Hearing Loss--genetics--United Arab Emirates. 
<br/><br/><label>National Library of Medicine Call No.: </label>WV270  / AL453c 2019