Page last updated: 2024-08-25

n-formylglycine and Sphingolipid Storage Diseases

n-formylglycine has been researched along with Sphingolipid Storage Diseases in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (100.00)2.80

Authors

AuthorsStudies
Adang, LA; Ahrens-Nicklas, RC; Radhakrishnan, K; Schlotawa, L1

Reviews

1 review(s) available for n-formylglycine and Sphingolipid Storage Diseases

ArticleYear
Multiple Sulfatase Deficiency: A Disease Comprising Mucopolysaccharidosis, Sphingolipidosis, and More Caused by a Defect in Posttranslational Modification.
    International journal of molecular sciences, 2020, May-13, Volume: 21, Issue:10

    Topics: Glycine; Humans; Mucopolysaccharidoses; Multiple Sulfatase Deficiency Disease; Mutation; Oxidoreductases Acting on Sulfur Group Donors; Protein Processing, Post-Translational; Sphingolipidoses; Sulfatases

2020