Associated Papers
Next-generation sequencing improves precision medicine in hearing loss.
Imizcoz T et al.
Frontiers in Genetics, 2023
Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases.
Audo I et al.
Orphanet Journal of Rare Diseases, 2012
Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse origin.
Aller E et al.
Molecular Vision, 2010
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