Next-generation sequencing for genetic testing of hearing loss populations
CONCLUSION: Our findings expand the mutation spectrum of hearing loss and highlight the importance of genetic diagnosis and prenatal diagnosis to allow accurate and personalized guidance for those at high risk of deafness.PMID:38056549 | DOI:10.1016/j.cca.2023.117693
Source: International Journal of Clinical Chemistry - Category: Chemistry Authors: Lulu Wang Gang Liu Dingyuan Ma Huasha Zeng Yuguo Wang Chunyu Luo Jingjing Zhang Zhengfeng Xu Source Type: research