A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60
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| Description | scientific article |
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author: Bouthaina Hammami Mhamed Grati Noritaka Nakamichi Mariem Ben Saïd Mustafa Tekin |
| Publication date | March 29, 2016 |
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| Missing/wrong data? | Edit Wikidata item |