Page last updated: 2024-10-18

glycine and Inclusion Body Myopathy, Sporadic

glycine has been researched along with Inclusion Body Myopathy, Sporadic 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
Djamshidian, A1
Schaefer, J1
Haubenberger, D1
Stogmann, E1
Zimprich, F1
Auff, E1
Zimprich, A1

Other Studies

1 other study available for glycine and Inclusion Body Myopathy, Sporadic

ArticleYear
A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia.
    Muscle & nerve, 2009, Volume: 39, Issue:3

    Topics: Adenosine Triphosphatases; Adult; Arginine; Cell Cycle Proteins; Dementia; DNA Mutational Analysis;

2009