MOESM5 of Recurrent NUS1 canonical splice donor site mutation in two unrelated individuals with epilepsy, myoclonus, ataxia and scoliosis - a case report
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https://springernature.figshare.com/articles/MOESM5_of_Recurrent_NUS1_canonical_splice_donor_site_mutation_in_two_unrelated_individuals_with_epilepsy_myoclonus_ataxia_and_scoliosis_-_a_case_report/10058972/1
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资源简介：
Additional file 5: Table S1. Process of variant filtering for patient 1.
提供机构：
figshare
创建时间：
2019-10-28
