F13A1 Sequencing

Mutations in F13A1 result in factor XIIIA deficiency, which is characterized by increased bleeding and poor wound healing. This condition is inherited in an autosomal recessive manner. This laboratory performs Sanger sequencing of the F13A1 gene.

Forms & Docs

Ordering

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Test Code
S0218

Turn Around Time
3-5 weeks

Billing

CPT Code
81479×1

Ordering Guidance

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

Details

Genes Covered
F13A1

Methods
Sanger