Lonneke Haer-Wigman Selected Research

Mucopolysaccharidosis III (Sanfilippo Syndrome)

7/2015

Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT).

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Lonneke Haer-Wigman Research Topics

Disease

3	Retinitis Pigmentosa (Pigmentary Retinopathy) 01/2019 - 07/2015
2	Macular Degeneration (Age-Related Maculopathy) 11/2021 - 01/2019
2	Retinal Degeneration 01/2018 - 07/2015
1	Vision Disorders (Hemeralopia) 11/2022
1	Cone-Rod Dystrophies 01/2019
1	Microcephaly 01/2018
1	Glomerulonephritis 01/2018
1	Retinal Dystrophies 01/2018
1	Ciliopathies 01/2017
1	Mucopolysaccharidosis III (Sanfilippo Syndrome) 07/2015

Drug/Important Bio-Agent (IBA)

2	Proteins (Proteins, Gene)FDA Link 01/2018 - 01/2017
1	NucleotidesIBA 11/2022
1	chemotactic factor inactivatorIBA 11/2021
1	RNA Precursors (Precursor, mRNA)IBA 01/2019
1	N 30IBA 01/2019
1	ProteomeIBA 01/2018
1	Retinaldehyde (Retinal)IBA 01/2017
1	AcetyltransferasesIBA 07/2015