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Identification of the causative mutation for leopard complex spotting and congenital stationary night blindness in equines and a method for testing for same
Identification of the causative mutation for leopard complex spotting and congenital stationary night blindness in equines and a method for testing for same
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机译:马中豹类复合物斑点和先天性静止性夜盲的致病突变的鉴定及其检测方法
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摘要
Methods are provided for determining whether or not a horse is genetically normal, is a carrier of, or is affected with or predisposed to Congenital Stationary Night Blindness and/or leopard complex spotting. The method is based on detection of an insertion in an intron in the horse Transient Receptor Potential Cation Channel, Subfamily M, Member 1 (TRPM1) gene.
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