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Hereditary Deafness Gene Detection (227 Genes+Mitochondrial Genome) CapitalBio

This test is based on NGS technology, it can detect 227 nuclear genomes + mitochondrial genome sequence, covering reported non-syndromic deafness and syndrome deafness.

rna seq fusion detection

Clinical Applications of Hereditary Deafness Gene Detection (227 Genes+Mitochondrial Genome)

  • Auxiliary diagnosis: search for the cause of suspected hereditary deafness and assist clinical diagnosis.

  • Disease risk assessment: conduct risk assessment for high-risk groups with family history and provide early intervention programs to reduce the risk of disease.


 


Specification of Hereditary Deafness Gene Detection (227 Genes+Mitochondrial Genome)

Sample typeVenous Blood/ Dried Blood Spot
TAT20 days


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