Heterozygous individuals in ABCA4 disease and control cohort harboring rare variants in macular dystrophy genes CDHR1, CHM, CRX, ELOVL4, PROM1, PRPH2, ROM1.
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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
