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