threonine and Hemophilia A

threonine has been researched along with Hemophilia A in 2 studies

Research

Studies (2)

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

Authors

Authors	Studies
Ewenstein, BM; Gorlin, J; Handin, RI; Jesson, M; Narins, SC; Wise, RJ	1
Brayer, GD; Geddes, VA; Le Bonniec, BF; Louie, GV; MacGillivray, RT; Thompson, AR	1

Reviews

1 review(s) available for threonine and Hemophilia A

Article	Year
Autosomal recessive transmission of hemophilia A due to a von Willebrand factor mutation. Human genetics, 1993, Volume: 91, Issue:4 Topics: Base Sequence; Diagnosis, Differential; DNA Mutational Analysis; Factor VIII; Female; Genes, Recessive; Hemophilia A; Humans; Infant; Methionine; Molecular Sequence Data; Pedigree; Point Mutation; Precipitin Tests; Protein Binding; Threonine; von Willebrand Diseases; von Willebrand Factor	1993

Article

Year

Autosomal recessive transmission of hemophilia A due to a von Willebrand factor mutation.

Human genetics, 1993, Volume: 91, Issue:4

Topics: Base Sequence; Diagnosis, Differential; DNA Mutational Analysis; Factor VIII; Female; Genes, Recessive; Hemophilia A; Humans; Infant; Methionine; Molecular Sequence Data; Pedigree; Point Mutation; Precipitin Tests; Protein Binding; Threonine; von Willebrand Diseases; von Willebrand Factor

1993

Other Studies

1 other study(ies) available for threonine and Hemophilia A

Article	Year
A moderate form of hemophilia B is caused by a novel mutation in the protease domain of factor IXVancouver. The Journal of biological chemistry, 1989, Mar-15, Volume: 264, Issue:8 Topics: Amino Acid Sequence; Base Sequence; Cloning, Molecular; Codon; DNA; DNA Probes; Exons; Factor IX; Factor IXa; Hemophilia A; Humans; Introns; Isoleucine; Lymphocytes; Molecular Sequence Data; Molecular Weight; Mutation; Nucleic Acid Hybridization; Serine Endopeptidases; Threonine	1989

Article

Year

A moderate form of hemophilia B is caused by a novel mutation in the protease domain of factor IXVancouver.

The Journal of biological chemistry, 1989, Mar-15, Volume: 264, Issue:8

Topics: Amino Acid Sequence; Base Sequence; Cloning, Molecular; Codon; DNA; DNA Probes; Exons; Factor IX; Factor IXa; Hemophilia A; Humans; Introns; Isoleucine; Lymphocytes; Molecular Sequence Data; Molecular Weight; Mutation; Nucleic Acid Hybridization; Serine Endopeptidases; Threonine

1989