Borderline plasma factor X (FX) levels might complicate the diagnosis of FX deficiency. An asymptomatic individual with 73% FX activity was identified to be heterozygous for the Val342Ala mutation. Expression studies suggested that this substitution is responsible for a CRM+ FX variant with normal activation but modestly reduced catalytic function.

Molecular characterization of factor X deficiency associated with borderline plasma factor X level

PINOTTI, Mirko;BARONI, Marcello;MARCHETTI, Giovanna;BERNARDI, Francesco
2004

Abstract

Borderline plasma factor X (FX) levels might complicate the diagnosis of FX deficiency. An asymptomatic individual with 73% FX activity was identified to be heterozygous for the Val342Ala mutation. Expression studies suggested that this substitution is responsible for a CRM+ FX variant with normal activation but modestly reduced catalytic function.
2004
Pinotti, Mirko; Monti, M; Baroni, Marcello; Marchetti, Giovanna; Bernardi, Francesco
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1197686
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