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)
Copyright policy ) Giridhara R. Jayandharan; Mammen Chandy; Sukesh Chandran Nair; Arun Srivastava; R. V. Shaji;
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)
Male, Genotype, Factor XI Deficiency, Phenylalanine, Mutation, Missense, Hemorrhage, Exons, Hemophilia B, Polymerase Chain Reaction, Introns, Factor IX, Phenotype, Leucine, Mutation, Humans, Female, Child, Codon, Factor XI, DNA Primers
Male, Genotype, Factor XI Deficiency, Phenylalanine, Mutation, Missense, Hemorrhage, Exons, Hemophilia B, Polymerase Chain Reaction, Introns, Factor IX, Phenotype, Leucine, Mutation, Humans, Female, Child, Codon, Factor XI, DNA Primers
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Citations provided by BIP!
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
Citations provided by BIP!popularityPopularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
Popularity provided by BIP! 13
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