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DMWD (DM1 Locus, WD Repeat Containing) is a Protein Coding gene. Diseases associated with DMWD include Myotonic Dystrophy 1 and Corticosteroid Allergy. An important paralog of this gene is WDR20. [GeneCards]
D19S593E; Dm9; DMRN9; DMR-N9; DMWD; dystrophia myotonica linked gene, N9; dystrophia myotonica WD repeat-containing protein; dystrophia myotonica, WD repeat containing; dystrophia myotonica-containing WD repeat motif; dystrophia myotonica-containing WD repeat motif protein; gene59; Protein 59; Protein DMR-N9
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100 µL