初売り cause variants SPTBN1 Pathogenic an dominant autosomal 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 12inch UK盤/DJ QUICKSILVER BELLISSIMA 新米 令和6年 【きぬむすめ】20kg 静岡県産 精米