SLC9A6 Sequencing
Test Background
Mutations in SLC9A6 can cause microcephaly, impaired ocular movement, severe global developmental delay, developmental regression, hypotonia, abnormal movements, and early-onset seizures. It is an X-linked condition. Carrier females may be mildly affected. This laboratory performs Sanger sequencing of the SLC9A6 gene.
Gene(s)
SLC9A6