A Novel Point Variant inNTRK3, R645C, Suggests a Role of this Gene in the Pathogenesis of Hirschsprung Disease

Title
A Novel Point Variant inNTRK3, R645C, Suggests a Role of this Gene in the Pathogenesis of Hirschsprung Disease
Authors
Keywords
-
Journal
ANNALS OF HUMAN GENETICS
Volume 73, Issue 1, Pages 19-25
Publisher
Wiley
Online
2009-01-03
DOI
10.1111/j.1469-1809.2008.00479.x

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