CLN3 Polyclonal Antibody, 50ul Centrifugal Filter Some patients also develop Cockayne

Some patients also develop Cockayne syndrome

Mutations in TUBA1A cause lissencephaly type 3 (LIS3) - a neurological condition characterized by microcephaly

and thus play an important role in protecting cells from oxidative stress

LMX1B encodes a member of LIM-homeodomain family of proteins containing two N-terminal zinc-binding LIM domains

These receptors are heteromeric protein complexes with multiple subunits

CLN3 Polyclonal Antibody, 50ul Centrifugal Filter Some patients also develop CockayneThis gene encodes a protein that is involved in lysosomal function. Mutations in this, as well as other neuronal ceroid lipofuscinosis (CLN) genes, cause neurodegenerative diseases commonly known as Batten disease or collectively known as neuronal ceroid lipofuscinoses (NCLs). Many alternatively spliced transcript variants have been found for this gene.