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An APRT mutation is strongly associated with and likely causative for 2,8-dihydroxyadenine urolithiasis in dogs()
2,8-Dihydroxyadenine (2,8-DHA) urolithiasis in people is caused by autosomal recessive mutations in the adenine phosphoribosyltransferase gene (APRT). 2,8-DHA urolithiasis has recently been reported in two dogs, but, to the authors’ knowledge, no studies have yet investigated the genetic basis for s...
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| Publié dans: | Mol Genet Metab |
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| Auteurs principaux: | , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2013
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4314209/ https://ncbi.nlm.nih.gov/pubmed/24359665 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2013.12.002 |
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