Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss

Overview of attention for article published in Journal of Translational Medicine, November 2014

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So far, Dimensions has found 37 publications that cite this research output.

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The most recent citing publications are shown below. View all 37 publications that cite this research output on Dimensions.

Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review

Article in Biomedicines (June 2023)

Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses

Article in European Journal of Human Genetics (April 2023)

WFS1 autosomal dominant variants linked with hearing loss: update on structural analysis and cochlear implant outcome

Article in BMC Medical Genomics (April 2023)

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