n-formylglycine has been researched along with Sphingolipid Storage Diseases 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 | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (100.00) | 2.80 |
Authors | Studies |
---|---|
Adang, LA; Ahrens-Nicklas, RC; Radhakrishnan, K; Schlotawa, L | 1 |
1 review(s) available for n-formylglycine and Sphingolipid Storage Diseases
Article | Year |
---|---|
Multiple Sulfatase Deficiency: A Disease Comprising Mucopolysaccharidosis, Sphingolipidosis, and More Caused by a Defect in Posttranslational Modification.
Topics: Glycine; Humans; Mucopolysaccharidoses; Multiple Sulfatase Deficiency Disease; Mutation; Oxidoreductases Acting on Sulfur Group Donors; Protein Processing, Post-Translational; Sphingolipidoses; Sulfatases | 2020 |