PM34 Polyclonal Antibody, 20ul Peptide Library a condition characterized by mild

a condition characterized by mild mental retardation

preimplantation embryos

Acetylcholinesterase exists in multiple molecular forms which possess similar catalytic properties| but differ in their oligomeric assembly and mode of cell attachment to the cell surface

an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome

Huntingtin is a disease gene linked to Huntington's disease| a neurodegenerative disorder characterized by loss of striatal neurons

PM34 Polyclonal Antibody, 20ul Peptide Library a condition characterized by mildThis gene encodes a peroxisomal membrane protein that belongs to the family of mitochondrial solute carriers. It is expressed in the liver, and is likely involved in transport. Alternative splicing results in multiple transcript variants.