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Journal of Medical Genetics logoLink to Journal of Medical Genetics
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. 2001 Aug;38(8):e25. doi: 10.1136/jmg.38.8.e25

A novel mutation in a family with non-syndromic sensorineural hearing loss that disrupts the newly characterised OTOF long isoforms

M Houseman, A Jackson, L Al-Gazali, R Badin, E Roberts, R Mueller
PMCID: PMC1734926  PMID: 11483641

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