This page, "ethylheptyl-amine", is part of the NIST Chemistry WebBook. This site and its contents are part of the NIST Standard Reference Data Program.
clinical testing for patients with epilepsy and development delay. A trio-whole exome sequencing revealed a novel homozygous frameshift variant in CNTN2 (c.2873_c.2874delCT, p.Thr958Thrfs) . SNP mutat
