Ataxin-1 Polyclonal Antibody, 100ul Filtration Mutations in this gene are

Mutations in this gene are associated with Warburg micro syndrome type 3

The related mouse protein was also shown to inhibit activating transcription factor 4-mediated transcription and thus regulate bone mass accrual

and susceptibility to osteoarthritis

Mutations in ADAMTS18 may be associated with microcornea

This gene encodes a member of a family of p21-stimulated serine/threonine protein kinases

Ataxin-1 Polyclonal Antibody, 100ul Filtration Mutations in this gene areThe autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always