CNNM2

Publications

Arjona FJ et al. CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemia. PLoS Genet. 2014;10(4).  PMID: 24699222.

Stuiver M et al. CNNM2, encoding a basolateral protein required for renal Mg2+ handling, is mutated in dominant hypomagnesemia. Am J Hum Genet. 2011;88(3):33-43.  PMID: 21397062.

De Baaij JH et al. Membrane topology and intracellular processing of cyclin M2 (CNNM2). J Biol Chem. 2012;287(17):13644-13655.  PMID: 22399287.