SLC9A6 Sequencing

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.

Forms & Docs

Ordering

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Test Code
S0968

Turn Around Time
2-3 weeks

Billing

CPT Code
81406×1

Ordering Guidance

If there are questions regarding this test, please contact Client Services at 617-553-5880 or clientservices@claritasgenomics.com

Details

Genes Covered
SLC9A6

Methods
Sanger