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. Author manuscript; available in PMC: 2010 Mar 11.
Published in final edited form as: Prog Biophys Mol Biol. 2009 Jan 30;98(2-3):149–160. doi: 10.1016/j.pbiomolbio.2009.01.012

Figure 2.

Figure 2

Schematic of CAV3 mutations associated with cardiac phenotype genetic diseases. Shown are locations of Cav-3 mutations identified in of Long QT syndrome type 9 (LQT9; red), sudden infant death syndrome (SIDS; pink) and hypertrophic cardiomyopathy (orange) patients. Mutation T78M in the membrane insertion region of the Cav3 was found to be associated with cases of both LQT9 and SIDS.