NMDAEpsilon3 Polyclonal Antibody, 100ul Molecular Biologyn Mutations in this gene cause

Mutations in this gene cause Schwartz-Jampel syndrome type 2

and in this way plays a role in innate immune response

Diseases associated with SLC7A4 include velocardiofacial syndrome and chromophobe adenoma

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NMDAEpsilon3 Polyclonal Antibody, 100ul Molecular Biologyn Mutations in this gene causeGRIN2C encodes a subunit of the N methyl D aspartate (NMDA) receptor, which is a subtype of ionotropic glutamate receptor. NMDA receptors are found in the central nervous system, are permeable to cations and have an important role in physiological processes such as learning, memory, and synaptic development. The receptor is a tetramer of different subunits (typically heterodimer of subunit 1 with one or more of subunits 2A D), forming a channel that