glycine has been researched along with Inclusion Body Myopathy, Sporadic 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 |
---|---|
Djamshidian, A | 1 |
Schaefer, J | 1 |
Haubenberger, D | 1 |
Stogmann, E | 1 |
Zimprich, F | 1 |
Auff, E | 1 |
Zimprich, A | 1 |
1 other study available for glycine and Inclusion Body Myopathy, Sporadic
Article | Year |
---|---|
A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia.
Topics: Adenosine Triphosphatases; Adult; Arginine; Cell Cycle Proteins; Dementia; DNA Mutational Analysis; | 2009 |