最終決算 Pathogenic dominant autosomal an cause variants SPTBN1 トランス
Pathogenic SPTBN1 variants cause an autosomal dominant,Mutations in SLC39A14 disrupt manganese homeostasis and,Impaired neuronal KCC2 function by biallelic SLC12A5,Evaluating the clinical efficacy of a long-read sequencing,Frontiers | Novel CNNM2 Mutation Responsible for Autosomal 90s トランス 12 Omnigloae mind out ep Now Records 管理番号d2ymr2000 備蓄王 無洗米 長期保存米5kg + 炊飯用袋 35枚✴︎21