Associated Papers
Genetic etiological analysis of auditory neuropathy spectrum disorder by next-generation sequencing.
Sun L et al.
Frontiers in Neurology, 2022
The Many Faces of DFNB9: Relating OTOF Variants to Hearing Impairment.
Vona B et al.
Genes, 2020
The ChinaMAP analytics of deep whole genome sequences in 10,588 individuals.
Cao Y et al.
Cell Research, 2020
32355288 (PubMed )
Supplement: 41422_2020_322_MOESM14_ESM.xlsx › S7
Clinical and genetic study of 12 Chinese Han families with nonsyndromic deafness.
Wu D et al.
Molecular Genetics & Genomic Medicine, 2020
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