Whole exome sequencing identified a homozygous novel variant in DOP1A gene in the Pakistan family with neurodevelopmental disabilities
收藏DataCite Commons2023-10-13 更新2024-08-18 收录
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https://figshare.com/articles/dataset/Whole_exome_sequencing_identified_a_homozygous_novel_variant_in_DOP1A_gene_in_the_Pakistan_family_with_neurodevelopmental_disabilities_Case_report_and_literature_review/24285979
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资源简介：
Our study reveals the potential pathway of the myelinogenesis relevant NDDs and identifies DOP1A as a potential NDDs-relevant gene in human.
提供机构：
figshare
创建时间：
2023-10-11
