WDR73 抗体
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Latest Publications for our WDR73 抗体
: "Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73. ..." in: Brain : a journal of neurology, Vol. 138, Issue Pt 8, pp. 2173-90, (2015) (PubMed).Aliases for WDR73 抗体
WD repeat domain 73 (WDR73) 抗体WD repeat domain 73 (Wdr73) 抗体
WD repeat domain 73 L homeolog (wdr73.L) 抗体
WD repeat domain 73 (wdr73) 抗体
1200011I23Rik 抗体
2410008B13Rik 抗体
AI848574 抗体
C85352 抗体
zgc:112071 抗体