Web: | mayocliniclabs.com |
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Email: | mcl@mayo.edu |
Telephone: | 800-533-1710 |
International: | +1 855-379-3115 |
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Aiding in the diagnosis of hereditary paraganglioma-pheochromocytoma syndrome associated with SDHB, SDHC, and SDHD gene mutations
Testing includes full gene sequencing of the SDHB, SDHC, SDHD genes and multiplex ligation-dependent probe amplification for the detection of large deletions and duplications within the SDHB, SDHC, SDHD genes.
Polymerase Chain Reaction (PCR) Followed by DNA Sequence Analysis and Gene Dosage Analysis by Multiplex Ligation-Dependent Probe Amplification (MLPA)