A multiplex PCR amplicon sequencing assay to screen genetic hearing loss variants in newborns

BACKGROUND: Congenital hearing loss is one of the most common birth defects. Early identification and management play a crucial role in improving patients’ communication and language acquisition. Previous studies demonstrated that genetic screening complements newborn hearing screening in clinical s...

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Detalles Bibliográficos
Autores principales: Yang, Haiyan, Luo, Hongyu, Zhang, Guiwei, Zhang, Junqing, Peng, Zhiyu, Xiang, Jiale
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913202/
https://www.ncbi.nlm.nih.gov/pubmed/33639928
http://dx.doi.org/10.1186/s12920-021-00906-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913202/
https://www.ncbi.nlm.nih.gov/pubmed/33639928
http://dx.doi.org/10.1186/s12920-021-00906-1

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