Select SNVs from patients 1 and 2.
收藏Figshare2015-12-03 更新2026-04-29 收录
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https://figshare.com/articles/dataset/_Select_SNVs_from_patients_1_and_2_/1350418
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NF2 loss-of-function mutations were common to both patients, as well as mutations in CNTNAP3B (shown in bold). For a complete list of SNVs see S1 File and S2 File.Select SNVs from patients 1 and 2.
创建时间：
2015-12-03
