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美国阿拉伯马中重症联合免疫缺陷(SCID)基因的频率。

Frequency of the SCID gene among Arabian horses in the USA.

作者信息

Bernoco D, Bailey E

机构信息

Stormont Laboratories, Inc., Woodland, CA 95616, USA.

出版信息

Anim Genet. 1998 Feb;29(1):41-2. doi: 10.1046/j.1365-2052.1998.00237.x.

Abstract

Severe combined immunodeficiency disease (SCID) of horses is an autosomal, recessive hereditary disease occurring among Arabian horses. The genetic defect responsible for this disease was recently identified as a 5-basepair deletion in the gene encoding DNA-protein kinase catalytic subunit (DNA-PKcs). Horses with one copy of the gene appear normal, while horses with two copies of the gene manifest the disease. The present report describes a PCR-based test for detection of the gene defect and the results from testing 250 randomly selected Arabian horses. The frequency of SCID gene carriers was 8.4% (21/250). Based on the gene frequency reported here, the authors would expect 0.18% (1 out of 567) of Arabian foals to be affected with SCID based on a random breeding population.

摘要

马的重症联合免疫缺陷病(SCID)是一种常染色体隐性遗传病,发生于阿拉伯马中。最近确定,导致这种疾病的基因缺陷是编码DNA蛋白激酶催化亚基(DNA-PKcs)的基因中一个5碱基对的缺失。携带该基因一个拷贝的马看起来正常,而携带两个拷贝的马则会表现出这种疾病。本报告描述了一种基于聚合酶链反应(PCR)的检测该基因缺陷的方法以及对250匹随机挑选的阿拉伯马进行检测的结果。SCID基因携带者的频率为8.4%(21/250)。根据此处报告的基因频率,作者预计在随机繁殖的种群中,0.18%(567匹中有1匹)的阿拉伯马驹会患SCID。

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