Flexible Real-Time Polymerase Chain Reaction-Based Platforms for Detecting Deafness Mutations in Koreans: A Proposed Guideline for the Etiologic Diagnosis of Auditory Neuropathy Spectrum Disorder

Routine application of next-generation sequencing in clinical settings is often limited by time- and cost-prohibitive complex filtering steps. Despite the previously introduced genotyping kit that allows screening of the 11 major recurring variants of sensorineural hearing loss (SNHL) genes in the K...

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Detalles Bibliográficos
Autores principales: Lee, Sang-Yeon, Oh, Doo-Yi, Han, Jin Hee, Kim, Min Young, Kim, Bonggi, Kim, Bong Jik, Song, Jae-Jin, Koo, Ja-Won, Lee, Jun Ho, Oh, Seung Ha, Choi, Byung Yoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7554951/
https://www.ncbi.nlm.nih.gov/pubmed/32899707
http://dx.doi.org/10.3390/diagnostics10090672

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7554951/
https://www.ncbi.nlm.nih.gov/pubmed/32899707
http://dx.doi.org/10.3390/diagnostics10090672

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