tryptophan and Becker Muscular Dystrophy

tryptophan has been researched along with Becker Muscular Dystrophy 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
Comi, GP; Connolly, A; Dasouki, M; Del Bo, R; Dunn, DM; Finkel, R; Flanigan, KM; Howard, MT; Jacobson, R; Medne, L; Mendell, J; Modrcin, A; Pickart, A; Saunders, C; von Niederhausern, A; Weiss, RB1

Other Studies

1 other study(ies) available for tryptophan and Becker Muscular Dystrophy

ArticleYear
DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy.
    Neuromuscular disorders : NMD, 2009, Volume: 19, Issue:11

    Topics: Adolescent; Child; Child, Preschool; Chromosomes, Human, X; Codon, Nonsense; Dystrophin; Exons; Family Health; Female; Founder Effect; Genome-Wide Association Study; Humans; Italy; Male; Middle Aged; Muscular Dystrophy, Duchenne; North America; Tryptophan; Young Adult

2009