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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

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