FGF-17 Polyclonal Antibody, 100ul Nucleic Acid Amplification Defects in this gene are

Defects in this gene are a cause of Leigh syndrome

COX19 encodes a cytochrome c oxidase (COX)-assembly protein

SUGP2 encodes a member of the arginine/serine-rich family of splicing factors

This gene is identified by the similarity of its product to the N-terminal region of BCL7A protein

This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate

FGF-17 Polyclonal Antibody, 100ul Nucleic Acid Amplification Defects in this gene areFGF17 encodes a member of the fibroblast growth factor (FGF) family. Member of the FGF family possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes including embryonic development cell growth, morphogenesis, tissue repair, tumor growth and invasion. Fibroblast growth factor 17 is expressed during embryogenesis and in the adult cerebellum and cortex and may be essential for vascular growth and