glycine has been researched along with Classic Globoid Cell Leukodystrophy in 1 studies
Excerpt | Relevance | Reference |
---|---|---|
"Krabbe disease (globoid cell leukodystrophy) is an autosomal recessive neurodegenerative disorder that affects both the central and peripheral nervous system due to an enzymatic defect of galactocerebrosidase (GALC)." | 1.30 | Molecular heterogeneity of Krabbe disease. ( Fu, L; Inui, K; Kokubu, C; Muramatsu, T; Nishigaki, T; Okada, S; Tatsumi, N; Tsukamoto, H, 1999) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Fu, L | 1 |
Inui, K | 1 |
Nishigaki, T | 1 |
Tatsumi, N | 1 |
Tsukamoto, H | 1 |
Kokubu, C | 1 |
Muramatsu, T | 1 |
Okada, S | 1 |
1 other study available for glycine and Classic Globoid Cell Leukodystrophy
Article | Year |
---|---|
Molecular heterogeneity of Krabbe disease.
Topics: Alanine; Animals; Blotting, Northern; COS Cells; DNA, Complementary; Galactosylceramidase; Gene Dele | 1999 |