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hypomagnesemia
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TRPM6
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family
CLDN16
Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption
EGF
The epidermal growth factor
CLDN19
A systems proteomics view of the endogenous human claudin protein family
FXYD2
Cloning and expression of human cDNA encoding Na+, K(+)-ATPase gamma-subunit
Cancer Gene Census
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Definition
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Pathways
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Signaling by EGFR
species not specified
one gene
egf signaling pathway
species not specified
one gene
role of egf receptor transactivation by gpcrs in cardiac hypertrophy
species not specified
one gene
keratinocyte differentiation
species not specified
one gene
Clinical Trials
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