Atrophin-1 Polyclonal Antibody, 100ul Cell Dissociation This gene encodes a member

This gene encodes a member of the steroid-thyroid hormone-retinoid receptor superfamily

and swallowing

Mice lacking this gene exhibit cardiac valve disease

encoded by three different genes

The protein encoded by HNRNPDL has two RRM domains that bind to RNAs

Atrophin-1 Polyclonal Antibody, 100ul Cell Dissociation This gene encodes a memberDentatorubral pallidoluysian atrophy (DRPLA) is a rare neurodegenerative disorder characterized by cerebellar ataxia, myoclonic epilepsy, choreoathetosis, and dementia. The disorder is related to the expansion from 7 35 copies to 49 93 copies of a trinucleotide repeat (CAG CAA) within this gene. The encoded protein includes a serine repeat and a region of alternating acidic and basic amino acids, as well as the variable glutamine repeat. Alternative