CI016 Rabbit Polyclonal Antibody, 20ul Protein Research which include the product of

which include the product of this gene and the P54NRB/NONO and PSF/SFPQ proteins

Mutations in this gene result in epimerase-deficiency galactosemia| also referred to as galactosemia type 3| a disease characterized by liver damage| early-onset cataracts| deafness and mental retardation| with symptoms ranging from mild ('peripheral' form) to severe ('generalized' form)

The enzyme encoded by this gene is active on phenols

is a 68 amino acid cytoplasmic protein involved in cellular differentiation

This subunit interacts with TBP and with two other small subunits of TFIID

CI016 Rabbit Polyclonal Antibody, 20ul Protein Research which include the product of