Associated Papers
ARSK-Related Mucopolysaccharidosis Type 10.
Al Fahdi I et al.
American Journal of Medical Genetics. Part A, 2025
Mucopolysaccharidoses-What Clinicians Need to Know: A Clinical, Biochemical, and Molecular Overview.
Lipiński P et al.
Biomolecules, 2025
Further characterization of ARSK-related mucopolysaccharidosis type 10.
Uludağ Alkaya D et al.
American Journal of Medical Genetics. Part A, 2024
A novel homozygous missense variant in ARSK causes MPS X, a new subtype of mucopolysaccharidosis.
Sun M et al.
Genes & Diseases, 2024
38292179 (PubMed )
Supplement: mmc1.docx
Phenotypic expansion of ARSK-related mucopolysaccharidosis.
Rustad CF et al.
American Journal of Medical Genetics. Part A, 2022
Novel subtype of mucopolysaccharidosis caused by arylsulfatase K (ARSK) deficiency.
Verheyen S et al.
Journal of Medical Genetics, 2022
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