Additional file 1 of Exome sequencing revealed a novel homozygous variant in TRMT61 A in a multiplex family with atypical Cornelia de Lange Syndrome from Rwanda
收藏NIAID Data Ecosystem2026-05-02 收录
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Supplementary Material 1: Supplementary Figure 1: Superimposed three-dimensionalstructures of TRMT61 A.Greenand light blueshowing no significant structural changes. Supplementary Figure S2: TRMT61 A_orignal Western blots
创建时间：
2025-05-13
