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A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes… https://t.co/EiHcK4NirS
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60
Overview of attention for article published in Human Genetics, March 2016
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In the top 25% of all research outputs scored by Altmetric
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Good Attention Score compared to outputs of the same age (75th percentile)
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Good Attention Score compared to outputs of the same age and source (65th percentile)
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