May play a role in developmental myelination of peripheral nerves.
Slowed nerve conduction velocity
SNCV
Affected individuals present a reduction in nerve conduction velocities without any clinical signs of peripheral or central nervous system dysfunction. SNCV inheritance is autosomal dominant.
None
The disease is caused by variants affecting the gene represented in this entry.
Methylated at Gln-1338 by N6AMT1.
Proteins
151612Da
We found 1 product in 1 category