NTAL Polyclonal Antibody, 20ul Custom Peptide Synthesis It also may play a

It also may play a role in regulating the kinetics of signaling in the phototransduction cascade

Mutations in this gene can cause optic atrophy 10| with or without ataxia| mental retardation| and seizures

an autosomal recessive ciliopathy and neurological disorder

natural killer cells

and the PH domain interacts with phospholipids and is responsible for association of PSCDs with membranes

NTAL Polyclonal Antibody, 20ul Custom Peptide Synthesis It also may play aThis gene is one of the contiguous genes at 7q11. 23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein.