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Summary Anatomy Item Literature (7748) Expression Attributions Wiki
XB-ANAT-11

Papers associated with brain (and fxyd2)

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Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome., Mann N., J Am Soc Nephrol. March 1, 2021; 32 (3): 580-596.    

FXYD7, mapping of functional sites involved in endoplasmic reticulum export, association with and regulation of Na,K-ATPase., Crambert G., J Biol Chem. July 16, 2004; 279 (29): 30888-95.

Xenopus Na,K-ATPase: primary sequence of the beta2 subunit and in situ localization of alpha1, beta1, and gamma expression during pronephric kidney development., Eid SR., Differentiation. September 1, 2001; 68 (2-3): 115-25.            

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