FGF-16 Polyclonal Antibody, 50ul Bio-Reaction Tube Defects in this gene are

Defects in this gene are a cause of retinitis pigmentosa autosomal recessive (ARRP) disease

and the Golgi complex

Galectin-4 is restricted to small intestine

sensory/pain processing

thyroid hormone and vitamin D3 receptors

FGF-16 Polyclonal Antibody, 50ul Bio-Reaction Tube Defects in this gene areFGF16 encodes a member of a family of proteins that are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene is expressed in cardiac cells and is required for proper heart development. Mutation in this gene was also observed in individuals with metacarpal 4 5 fusion.