Varaico: Literature-Extracted Genetic Variants

Gene:HGSNAT
Variant:p.W403C
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HGSNAT

NM_152419.3:p.W403C

Associated Papers

Structure of the human heparan-α-glucosaminide N-acetyltransferase (HGSNAT).

Navratna V et al.

Elife, 2024

Structure of the human heparan-α-glucosaminide N-acetyltransferase (HGSNAT).

Navratna V et al.

Biorxiv : the Preprint Server for Biology, 2024

Molecular characterization of a large group of Mucopolysaccharidosis type IIIC patients reveals the evolutionary history of the disease.

Martins C et al.

Human Mutation, 2019

The Genetic Basis of Pericentral Retinitis Pigmentosa-A Form of Mild Retinitis Pigmentosa.

Comander J et al.

Genes, 2017

arrEYE: a customized platform for high-resolution copy number analysis of coding and noncoding regions of known and candidate retinal dystrophy genes and retinal noncoding RNAs.

Van Cauwenbergh C et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2017

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

Haer-Wigman L et al.

Human Molecular Genetics, 2015

Molecular characterization of MPS IIIA, MPS IIIB and MPS IIIC in Tunisian patients.

Ouesleti S et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry, 2011

Functional analysis of the HGSNAT gene in patients with mucopolysaccharidosis IIIC (Sanfilippo C Syndrome).

Fedele AO et al.

Human Mutation, 2010

Protein misfolding as an underlying molecular defect in mucopolysaccharidosis III type C.

Feldhammer M et al.

Plos One, 2009

Sanfilippo syndrome type C: mutation spectrum in the heparan sulfate acetyl-CoA: alpha-glucosaminide N-acetyltransferase (HGSNAT) gene.

Feldhammer M et al.

Human Mutation, 2009

Mutational analysis of the HGSNAT gene in Italian patients with mucopolysaccharidosis IIIC (Sanfilippo C syndrome). Mutation in brief #959. Online.

Fedele AO et al.

Human Mutation, 2007

Hypomorphic variants in inherited retinal and ocular diseases: A review of the literature with clinical cases.

Thuma TBT et al.

Survey of Ophthalmology, 0

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."