Levesque, Sebastien <br/><br/>
A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population.  [electronic resource] 

 -  BMC medical genetics  Aug 2012 
 - 72 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>1471-2350 
<br/><br/><label>Standard No.: </label>10.1186/1471-2350-13-72  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>ATPases Associated with Diverse Cellular Activities<br/>Adenosine Triphosphatases--genetics<br/>Base Sequence<br/>Female<br/>Founder Effect<br/>France--ethnology<br/>High-Throughput Nucleotide Sequencing<br/>Humans<br/>Male<br/>Mutation<br/>Quebec--epidemiology<br/>White People--genetics<br/>Zellweger Syndrome--enzymology