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SERCA pumps and human diseases.
Hovnanian A. Hovnanian A. Subcell Biochem. 2007;45:337-63. doi: 10.1007/978-1-4020-6191-2_12. Subcell Biochem. 2007. PMID: 18193643 Review.
Defects in ATP2A1 encoding SERCA1 cause recessive Brody myopathy, mutations in ATP2A2 coding for SERCA2 underlie a dominant skin disease, Darier disease and its clinical variants. ...
Defects in ATP2A1 encoding SERCA1 cause recessive Brody myopathy, mutations in ATP2A2 coding for SERCA2 underlie a dominant sk …