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Mutations in this gene can cause X-chromosomal non-specific mental retardation

This gene encodes a predicted transmembrane protein with a perinuclear Golgi-like distribution in fibroblasts

Genetic variation in this gene may be associated with susceptibility to hereditary essential tremor 1

DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP (class II-associated invariant chain peptide) molecule from the peptide binding site

PLS5 Polyclonal Antibody, 100ul Transporters Experience lightning-fast results and conquer