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Impaired secretion of carboxyl-terminal truncated factor VII due to an F7 nonsense mutation associated with FVII deficiency

Transcriptional RegulationF7 Nonsense MutationMendelian DisorderDisease MechanismGenetic DisorderGeneticsPathogenesisPathologyImpaired SecretionMolecular GeneticsDisease Gene IdentificationFvii DeficiencyGene ExpressionMedicineMolecular Signaling