tryptophan and Afibrinogenemia

tryptophan has been researched along with Afibrinogenemia 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
Malé, PJ; Neerman-Arbez, M; Rougemont, AL; Rubbia-Brandt, L; Spahr, L	1

Other Studies

1 other study(ies) available for tryptophan and Afibrinogenemia

Article	Year
Fibrinogen gamma375 arg-->trp mutation (fibrinogen aguadilla) causes hereditary hypofibrinogenemia, hepatic endoplasmic reticulum storage disease and cirrhosis. The American journal of surgical pathology, 2006, Volume: 30, Issue:7 Topics: Adult; Afibrinogenemia; Amino Acid Sequence; Amino Acid Substitution; Arginine; Endoplasmic Reticulum; Family Health; Fibrinogen; Hepatocytes; Humans; Inclusion Bodies; Liver; Liver Cirrhosis; Male; Middle Aged; Molecular Sequence Data; Mutation, Missense; Point Mutation; Tryptophan	2006

Article

Year

Fibrinogen gamma375 arg-->trp mutation (fibrinogen aguadilla) causes hereditary hypofibrinogenemia, hepatic endoplasmic reticulum storage disease and cirrhosis.

The American journal of surgical pathology, 2006, Volume: 30, Issue:7

Topics: Adult; Afibrinogenemia; Amino Acid Sequence; Amino Acid Substitution; Arginine; Endoplasmic Reticulum; Family Health; Fibrinogen; Hepatocytes; Humans; Inclusion Bodies; Liver; Liver Cirrhosis; Male; Middle Aged; Molecular Sequence Data; Mutation, Missense; Point Mutation; Tryptophan

2006