OTX2 Monoclonal Antibody, 100ul[BT-MCA0963] DNA Libraries Synthesis Defects in EHHADH are a

Defects in EHHADH are a cause of peroxisomal disorders such as Zellweger syndrome

Genome-wide association studies in some populations have found an association between polymorphisms in this gene and sporadic amyotrophic lateral sclerosis

Polymorphisms in this gene have been implicated in modifying risk of Parkinson disease

colon cancer and acute leukemia

OTX2 Monoclonal Antibody, 100ul[BT-MCA0963] DNA Libraries Synthesis Defects in EHHADH are aThis gene encodes a member of the bicoid subfamily of homeodomain containing transcription factors. The encoded protein acts as a transcription factor and plays a role in brain, craniofacial, and sensory organ development. The encoded protein also influences the proliferation and differentiation of dopaminergic neuronal progenitor cells during mitosis. Mutations in this gene cause syndromic microphthalmia 5 (MCOPS5) and combined pituitary hormone