(Q46223924)
Statements
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A novel point variant in NTRK3, R645C, suggests a role of this gene in the pathogenesis of Hirschsprung disease (English)
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R M Fernández
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A Sánchez-Mejías
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M D Mena
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M Ruiz-Ferrer
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M López-Alonso
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G Antiñolo
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S Borrego
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20 October 2008
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73
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1
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19-25
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Identifiers
1 reference