Additional file 3 of Clinical exome sequencing facilitates the understanding of genetic heterogeneity in Leber congenital amaurosis patients with variable phenotype in southern India
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https://springernature.figshare.com/articles/dataset/Additional_file_3_of_Clinical_exome_sequencing_facilitates_the_understanding_of_genetic_heterogeneity_in_Leber_congenital_amaurosis_patients_with_variable_phenotype_in_southern_India/14552114/1
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资源简介：
Additional file 3: Supplementary Table S3. Overview of exclusion and prioritization of variants to obtain pathogenic variant from clinical exome data.
提供机构：
Vijayalakshmi Perumalsamy; Sriee Viswarubhiny; Devarajan Bharanidharan; Periasamy Sundaresan; Ayyasamy Vanniarajan
创建时间：
2021-05-07
