SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype

Published 2009 View Full Article

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Title
SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype
Authors
Keywords
-
Journal
JOURNAL OF MEDICAL GENETICS
Volume 46, Issue 7, Pages 431-437
Publisher
BMJ
Online
2009-05-15
DOI
10.1136/jmg.2008.065474

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