€57,48 €47,50 excl. VAT
Mucopolysaccharidosis VII (MPS7) belongs to a group of genetic disorders of glycosaminglycan catabolism resulting in lysosomal storage.
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Specifications
| Breeds | |
|---|---|
| Organ | |
| specimen | Swab, Blood EDTA, Blood Heparin, Semen, Tissue |
General Information
Mucopolysaccharidosis VII (MPS7) belongs to a group of genetic disorders of glycosaminglycan catabolism resulting in lysosomal storage.
Clinical signs are corneal clouding and severe skeletal deformities. Affected cats are unable to ambulate at several weeks to months of age.
Additional information
Clinical features
References
Pubmed ID:
Omia ID:
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