Des mutations dans l’exon HSN2...

Des mutations dans l’exon HSN2 du gène WNK1 causent la neuropathie héréditaire sensitive et autonomique de type 2

Rivière, Jean-Baptiste, Dion, Patrick, Shekarabi, Masoud, Girard, Nathalie, Faivre, Laurence, Lafrenière, Ronald G., Samuels, Mark, Rouleau, Guy A.
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
25
Language:
french
Journal:
médecine/sciences
DOI:
10.1051/medsci/2009253235
Date:
March, 2009
File:
PDF, 151 KB
french, 2009
Conversion to is in progress
Conversion to is failed