WDR62 Rabbit Polyclonal Antibody, 20ul Cell Dissociation mutations in this gene and

mutations in this gene and the BBS8 gene are thought to play a minor role and mutations in chaperonin-like BBS genes are found to be a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population

POLR3E (Polymerase (RNA) III Subunit E) is a Protein Coding gene

and macular dystrophy syndrome (EEMS)

as well as fertility

WDR62 Rabbit Polyclonal Antibody, 20ul Cell Dissociation mutations in this gene andThis gene is proposed to play a role in cerebral cortical development. Mutations in this gene have been associated with microencephaly cortical malformations and mental retardation. Alternative splicing results in multiple transcript variants.