Whole Genome Sequencing Identifies Missense Mutation in GRM6 as the Likely Cause of Congenital Stationary Night Blindness in a Tennessee Walking Horse
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下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJEB36381
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资源简介：
To identify sequencing variant(s) causal for Congenital Stationary Night Blindness in a Tennessee Walking Horse, we performed whole genome sequencing of at least 20X coverage on the Nova-Seq platform.
创建时间：
2020-09-02
