Additional file 1: of Clinical phenotype of ASD-associated DYRK1A haploinsufficiency
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Variant information for known de novo DYRK1A mutation cases. Full variant information for previously published DYRK1A variants and patients seen at UW. Previously published cases identified by first author last name and UW cases denoted TXXX. Sheets organized by variant type: snvs/indels, cnvs, mosaic variants, and translocations/inversions. (XLSX 17Â kb)
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Tychele Turner创建时间：
2017-10-06
