NTAL Polyclonal Antibody, 20ul Custom Peptide Synthesis an autosomal recessive ciliopathy and

an autosomal recessive ciliopathy and neurological disorder

Designed with a flat cap and conical bottom

Mutations in this gene have been implicated in autosomal dominant Alzheimer disease and cerebroarterial amyloidosis (cerebral amyloid angiopathy)

Binds to neuroligins NLGN1

NTAL Polyclonal Antibody, 20ul Custom Peptide Synthesis an autosomal recessive ciliopathy andThis 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.