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Steatocystoma multiplex
KRT17 (keratin 17)
Mutations in KRT17 are identified first by examination of mutational hotspots from genomic DNA from buccal swabs. If no mutation is found on this preliminary screen, we perform complete sequencing of the coding region of KRT17.
Information Sheet, including prices and CPT codes
Genetic Test Sample Submission Form (Test Requisition Form) including Payment Options
KRT17, keratin, sebaceous cyst
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