Reish, Orit <br/><br/>
Founder mutation(s) in the RSPH9 gene leading to primary ciliary dyskinesia in two inbred Bedouin families.  [electronic resource] 

 -  Annals of human genetics  Mar 2010 
 - 117-25 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1469-1809 
<br/><br/><label>Standard No.: </label>10.1111/j.1469-1809.2009.00559.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Arabs--genetics<br/>Consanguinity<br/>Humans<br/>Kartagener Syndrome--genetics<br/>Mutation