Compounds > tryptophan

tryptophan and Glycogen Storage Disease Type V

tryptophan has been researched along with Glycogen Storage Disease Type V in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Arenas, J; Cabello, A; Campos, Y; Martín, MA; Rubio, JC; Vílchez, J1

Other Studies

1 other study(ies) available for tryptophan and Glycogen Storage Disease Type V

ArticleYear
Two homozygous mutations (R193W and 794/795 delAA) in the myophosphorylase gene in a patient with McArdle's disease.
    Human mutation, 2000, Volume: 15, Issue:3

    Topics: Adolescent; Amino Acid Sequence; Arginine; Base Sequence; Glycogen Storage Disease Type V; Humans; Male; Mutation; Phosphorylases; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Tryptophan

2000