Identification of genetic defects in families segregating rare eye disorders using next generation genomic tools
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下载链接：
https://www.ncbi.nlm.nih.gov/sra/SRP298871
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资源简介：
To delineate novel genetic loci linked with eye disorders in families segregating hereditary disorders of eye using whole genome SNP genotyping followed by discovery of novel gene using whole exome sequencing. Use of identified variants to establish genotype-phenotype correlation
创建时间：
2020-12-24
