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  • 検索条件 : 絞込み (MeSH = Genetic Diseases, Inborn / metabolism)
生物種 リソース名 タイトル
遺伝子材料 pBC111 (RDB15296) , pBCT-CCH1H (RDB15297). Essential, completely conserved glycine residue in the domain III S2-S3 linker of voltage-gated calcium channel alpha1 subunits in yeast and mammals.
ヒト・動物細胞 ATDC5(RCB0565) Axial Spondylometaphyseal Dysplasia Is Caused by C21orf2 Mutations.