tyrosine has been researched along with Alexander Disease in 1 studies
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 | Studies |
---|---|
Christen, HJ; Das, AM; Donnerstag, F; Hagedorn, M; Hartmann, H; Herchenbach, J; Ledaal, P; Lücke, T; Meins, M; Stephani, U | 1 |
1 other study(ies) available for tyrosine and Alexander Disease
Article | Year |
---|---|
Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander disease.
Topics: Age of Onset; Alanine; Alexander Disease; Cysteine; DNA Mutational Analysis; Exons; Female; Frontal Lobe; Glial Fibrillary Acidic Protein; Humans; Infant; Magnetic Resonance Imaging; Male; Mutation; Protein Structure, Tertiary; Tyrosine; Valine | 2007 |