arginine and Factor X Deficiency

arginine has been researched along with Factor X Deficiency in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Baidya, S; Chandy, M; George, B; Jayandharan, G; Nair, SC; Shaji, RV; Srivastava, A; Viswabandya, A	1

Other Studies

1 other study(ies) available for arginine and Factor X Deficiency

Article	Year
Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T-->G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin. Journal of thrombosis and haemostasis : JTH, 2005, Volume: 3, Issue:7 Topics: Arginine; Codon, Nonsense; CpG Islands; DNA Mutational Analysis; DNA Primers; Epitopes; Exons; Factor Va; Factor X; Factor X Deficiency; Frameshift Mutation; Heterozygote; Humans; India; Lysine; Models, Genetic; Models, Molecular; Mutation; Mutation, Missense; Nepal; Phenylalanine; Serine	2005

Article

Year

Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T-->G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin.

Journal of thrombosis and haemostasis : JTH, 2005, Volume: 3, Issue:7

Topics: Arginine; Codon, Nonsense; CpG Islands; DNA Mutational Analysis; DNA Primers; Epitopes; Exons; Factor Va; Factor X; Factor X Deficiency; Frameshift Mutation; Heterozygote; Humans; India; Lysine; Models, Genetic; Models, Molecular; Mutation; Mutation, Missense; Nepal; Phenylalanine; Serine

2005