leucine and Deficiency, Factor 11

leucine has been researched along with Deficiency, Factor 11 in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Choi, JR; Kim, J; Kim, Y; Lee, KA; Lyu, CJ; Shin, S	1
Chandy, M; Jayandharan, G; Nair, SC; Shaji, RV; Srivastava, A	1

Other Studies

2 other study(ies) available for leucine and Deficiency, Factor 11

Article	Year
A novel F11 mutation in a Korean pediatric patient with recurrent epistaxis. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 2013, Volume: 24, Issue:4 Topics: Amino Acid Sequence; Animals; Asian People; Base Sequence; Child; Epistaxis; Factor XI; Factor XI Deficiency; Heterozygote; Humans; Leucine; Male; Molecular Sequence Data; Mutation; Pedigree; Phenylalanine; Recurrence; Sequence Alignment	2013
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). Journal of thrombosis and haemostasis : JTH, 2005, Volume: 3, Issue:4 Topics: Child; Codon; DNA Primers; Exons; Factor IX; Factor XI; Factor XI Deficiency; Female; Genotype; Hemophilia B; Hemorrhage; Humans; Introns; Leucine; Male; Mutation; Mutation, Missense; Phenotype; Phenylalanine; Polymerase Chain Reaction; Serine; Tyrosine; Valine	2005

Article

Year

A novel F11 mutation in a Korean pediatric patient with recurrent epistaxis.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 2013, Volume: 24, Issue:4

Topics: Amino Acid Sequence; Animals; Asian People; Base Sequence; Child; Epistaxis; Factor XI; Factor XI Deficiency; Heterozygote; Humans; Leucine; Male; Molecular Sequence Data; Mutation; Pedigree; Phenylalanine; Recurrence; Sequence Alignment

2013

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).

Journal of thrombosis and haemostasis : JTH, 2005, Volume: 3, Issue:4

Topics: Child; Codon; DNA Primers; Exons; Factor IX; Factor XI; Factor XI Deficiency; Female; Genotype; Hemophilia B; Hemorrhage; Humans; Introns; Leucine; Male; Mutation; Mutation, Missense; Phenotype; Phenylalanine; Polymerase Chain Reaction; Serine; Tyrosine; Valine

2005