Page last updated: 2024-08-25

n-formylglycine and Xeroderma

n-formylglycine has been researched along with Xeroderma in 1 studies

Research

Studies (1)

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	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Babicz, M; Dierks, T; Jaszczuk, I; Koppenhöfer, D; Lejman, M; Ohlenbusch, A; Radhakrishnan, K; Schlotawa, L; Ługowska, A	1

Other Studies

1 other study(ies) available for n-formylglycine and Xeroderma

Article	Year
Expanding the genetic cause of multiple sulfatase deficiency: A novel SUMF1 variant in a patient displaying a severe late infantile form of the disease. Molecular genetics and metabolism, 2017, Volume: 121, Issue:3 Topics: Cells, Cultured; Child, Preschool; Computer Simulation; Enzymes; Glycine; Humans; Ichthyosis; Male; Multiple Sulfatase Deficiency Disease; Mutation, Missense; Oxidoreductases Acting on Sulfur Group Donors; Phenotype; Poland; Protein Processing, Post-Translational; Sulfatases	2017

Article

Year

Expanding the genetic cause of multiple sulfatase deficiency: A novel SUMF1 variant in a patient displaying a severe late infantile form of the disease.

Molecular genetics and metabolism, 2017, Volume: 121, Issue:3

Topics: Cells, Cultured; Child, Preschool; Computer Simulation; Enzymes; Glycine; Humans; Ichthyosis; Male; Multiple Sulfatase Deficiency Disease; Mutation, Missense; Oxidoreductases Acting on Sulfur Group Donors; Phenotype; Poland; Protein Processing, Post-Translational; Sulfatases

2017