Cav3.3 Polyclonal Antibody, 50ul Sealing Film Mutations in this gene cause

Mutations in this gene cause coenzyme Q10 deficiency| a mitochondrial encephalomyopathy| and also COQ2 nephropathy| an inherited form of mitochondriopathy with primary renal involvement

The T-box family members share a common DNA binding domain

Defects in this gene are a cause of glutathione synthetase deficiency

and this DMR is commonly found in imprinted genes and correlates with transcript expression

It contains an internal duplication of two catalytic domains which appear to function independently of each other

Cav3.3 Polyclonal Antibody, 50ul Sealing Film Mutations in this gene causeThis gene encodes the pore forming alpha subunit of a voltage gated calcium channel. The encoded protein is a member of a subfamily of calcium channels referred to as is a low voltage activated, T type, calcium channel. The channel encoded by this protein is characterized by a slower activation and inactivation compared to other T type calcium channels. This protein may be involved in calcium signaling in neurons. Alternate splicing results in