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A Novel Point Variant in NTRK3, R645C, Suggests a Role of this Gene in the Pathogenesis of Hirschsprung Disease

✍ Scribed by R. M. Fernández; A. Sánchez-Mejías; M. D. Mena; M. Ruiz-Ferrer; M. López-Alonso; G. Antiñolo; S. Borrego

Book ID: 111111460
Publisher: John Wiley and Sons
Year: 2009
Tongue: English
Weight: 215 KB
Volume: 73
Category: Article
ISSN: 0003-4800
DOI: 10.1111/j.1469-1809.2008.00479.x

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