Pseudoexon activation in thePKHD1gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney disease

Published 2009 View Full Article

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Title
Pseudoexon activation in thePKHD1gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney disease
Authors
Keywords
-
Journal
CLINICAL GENETICS
Volume 75, Issue 2, Pages 203-206
Publisher
Wiley
Online
2009-01-23
DOI
10.1111/j.1399-0004.2008.01106.x

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