Novel missense mutations in two patients with factor XI deficiency (Val271Leu and Tyr351Ser) and one patient with combined factor XI and factor IX deficiency (Phe349Val)

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Bibliographische Detailangaben
Veröffentlicht in:	Journal of thrombosis and haemostasis 2005-04, Vol.3 (4), p.808-811
Hauptverfasser:	JAYANDHARAN, G., SHAJI, R. V., NAIR, S. C., CHANDY, M., SRIVASTAVA, A.
Format:	Artikel
Sprache:	eng
Schlagworte:	Child Codon DNA Primers - chemistry Exons Factor IX - genetics Factor XI - genetics Factor XI Deficiency - genetics Female Genotype Hemophilia B - genetics Hemorrhage Humans Introns Leucine - chemistry Male Mutation Mutation, Missense Phenotype Phenylalanine - chemistry Polymerase Chain Reaction Serine - chemistry Tyrosine - chemistry Valine - chemistry
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