FibrinogenPoint MutationMutation, MissenseMutationAfibrinogenemiaFibrin Fibrinogen Degradation ProductsFrameshift MutationFibrinGerm-Line MutationFibrinopeptide BPedigreeFibrinopeptide AMolecular Sequence DataAmino Acid SequenceBase SequenceBlood PlateletsMutation RateHeterozygoteExonsAmino Acid SubstitutionPlatelet Membrane GlycoproteinsPlatelet AggregationPolymerase Chain ReactionAllelesBlood CoagulationDNA Mutational AnalysisThrombinMutagenesis, Site-DirectedThrombin TimeReceptors, FibrinogenPolymorphism, Single-Stranded ConformationalGenotypeHomozygoteBinding SitesPlatelet Glycoprotein GPIIb-IIIa ComplexBlood Coagulation DisordersProtein BindingCodon, NonsenseFibrinolysisMutagenesisSequence Analysis, DNABlood Coagulation TestsFibrinolysinProtein Structure, TertiaryHemostasisSequence DeletionGenes, RecessiveModels, MolecularPlatelet AdhesivenessKineticsCell LineDNA PrimersFactor XIIIGenes, DominantGenetic TestingPhenotypeAncrodEscherichia coliClot RetractionSequence Homology, Amino AcidBatroxobinSuppression, GeneticChromosome MappingCodonPlatelet ActivationRecombinant ProteinsAdenosine DiphosphateProtein ConformationBacterial ProteinsDNA-Binding ProteinsDNACloning, MolecularProthrombin TimeConsanguinityGene DeletionMembrane ProteinsTranscription FactorsPolymorphism, GeneticGenetic Complementation TestSequence AlignmentSyndromeGenetic Predisposition to DiseaseTransfectionFounder EffectGenes, p53Genetic LinkageStructure-Activity RelationshipMutant ProteinsBlood Coagulation FactorsElectrophoresis, Polyacrylamide GelPlasmidsBlood ViscosityCarrier ProteinsOligopeptidesvon Willebrand FactorGenetic VariationPlasminogenPeptide FragmentsThrombosisModels, Genetic