Additional file 6: Table S4. of Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis
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https://springernature.figshare.com/articles/dataset/Additional_file_6_Table_S4_of_Targeted_high-throughput_sequencing_for_genetic_diagnostics_of_hemophagocytic_lymphohistiocytosis/4444694/1
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资源简介：
Monoallelic rare variants with in silico pathogenic predictions identified in the patients without a definitive diagnosis. (XLSX 38 kb)
于未获得明确诊断的患者中鉴定出的、经计算机模拟致病性预测的单等位基因罕见变异（XLSX 38 KB）
提供机构：
Yenan Bryceson; Zuhre Kaya; Eya Bdira; Jan-Inge Henter; Sule Unal; Aysegul Unuvar
创建时间：
2016-12-15
