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THREE DIVERSE MUTATIONS UNDERLYING CANINE XANTHINE UROLITHIASIS

机译:甘氨酸黄嘌呤尿道潜在的三种不同突变

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Hereditary xanthinuria in people is an autosomal recessive disease caused by mutations in xanthine dehydrogenase (XDH) or molybdenum cofactor sulfurase (MOCOS). There are rare reports of hereditary xanthinuria in dogs, but genetic investigations havenot previously been described. The objective of this study was to identify mutations underlying risk for canine xanthine urolithiasis by sequencing XDH and MOCOS in affected dogs.
机译:人民遗传性黄嘌呤是一种由黄嘌呤脱氢酶(XDH)或钼壳硫酶(MOCOS)突变引起的常染色体隐性疾病。狗的遗传性黄嘌呤有罕见的报道,但之前已经描述了遗传调查。本研究的目的是通过测序XDH和MOCOS在受影响的狗的XDH和MOCOS鉴定犬黄嘌呤尿石病的突变风险。

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