Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses.
第一作者:
Rebecca R,Bellone
第一单位:
Department of Biology, University of Tampa, Tampa, FL 33611, USA. rbellone@ut.edu
作者:
医学主题词
动物(Animals);碱基序列(Base Sequence);染色体图(Chromosome Mapping);DNA突变分析(DNA Mutational Analysis);外显子(Exons);疾病遗传易感性(Genetic Predisposition to Disease);马疾病(Horse Diseases);马(Horses);分子序列数据(Molecular Sequence Data);夜盲(Night Blindness);多态性, 单核苷酸(Polymorphism, Single Nucleotide);启动区, 遗传(Promoter Regions, Genetic);TRPM阳离子通道(TRPM Cation Channels)
DOI
10.1093/bfgp/elq002
PMID
20353955
发布时间
2010-05-24
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