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
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https://figshare.com/articles/dataset/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/29079118
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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
