Associated Papers
Retinal Function Deficits in American Staffordshire Terriers with a Late-Onset Neurodegenerative Disease Associated with an ARSG Variant.
Kick GR et al.
Veterinary Sciences, 2025
PCR-based detection of hereditary mutations in SLC2A9, BTBD17, and NECAP1 among native Korean dog breeds.
Kang M et al.
Journal of Veterinary Science, 2025
40765230 (PubMed )
Supplement: jvs-26-e48-s001.xls › Supplementary_Table_1
Expanding the genetic landscape of Usher syndrome type IV caused by pathogenic ARSG variants.
Bauwens M et al.
Clinical Genetics, 2025
A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis.
Abitbol M et al.
Proceedings of the National Academy of Sciences of the United States of America, 2010
DNA testing in neurologic diseases.
O'Brien DP et al.
Journal of Veterinary Internal Medicine, 0
Phenotypic and genetic aspects of hereditary ataxia in dogs.
Stee K et al.
Journal of Veterinary Internal Medicine, 0
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