RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders

Published 2009 View Full Article

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Title
RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders
Authors
Keywords
-
Journal
CLINICAL GENETICS
Volume 74, Issue 2, Pages 164-170
Publisher
Wiley
Online
2009-01-23
DOI
10.1111/j.1399-0004.2008.01047.x

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