IndraLab

Statements

CACNA1G activates Cysteine proteinase inhibitor A. 3 / 3
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"SCA42 is a rare non-expansion SCA caused by mutations in CACNA1G on chromosome 17q21, encoding the pore-forming alpha1 subunit of the Ca(V)3.1, a low-threshold voltage-gated T-type calcium channel organized in four repeated domains (I-IV)."
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"Our study revealed that a mutation in CACNA1G encoding the T-type calcium channel Ca V 3.1 causes SCA."
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"SCA42 is a rare non-expansion SCA caused by mutations in CACNA1G on chromosome 17q21, encoding the Ca(V)3.1, a low-threshold voltage-gated T-type calcium channel."
39287920