Heterozygous individuals in ABCA4 disease and control cohort harboring rare variants in macular dystrophy genes CDHR1, CHM, CRX, ELOVL4, PROM1, PRPH2, ROM1.
收藏Figshare2022-03-30 更新2026-04-28 收录
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https://figshare.com/articles/dataset/Heterozygous_individuals_in_ABCA4_disease_and_control_cohort_harboring_rare_variants_in_macular_dystrophy_genes_i_CDHR1_i_i_CHM_i_i_CRX_i_i_ELOVL4_i_i_PROM1_i_i_PRPH2_i_i_ROM1_i_/19468900
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All comparisons were performed with the two-sided Fisher’s Exact Test (FET). MAF, minor allele frequency; gnomAD, genome aggregation database; CADD, combined annotation dependent depletion; nd, not detected.
创建时间：
2022-03-30
