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Hearing, Balance and Communication Volume 14, 2016 - Issue 1
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Original Article

Mutation screening of the Otop1 gene in familial benign positional paroxysmal vertigo

Daniele MonzaniOtolaryngology – Head and Neck Surgery Department, University Hospital of Modena, Modena, Italy
,
Tatiana FancelloDepartment of Biomedical Sciences, University of Modena and Reggio Emilia, Modena, Italy
,
Matteo Alicandri-CiufelliOtolaryngology – Head and Neck Surgery Department, University Hospital of Modena, Modena, Italy
,
Elisabetta GenoveseOtolaryngology – Head and Neck Surgery Department, University Hospital of Modena, Modena, Italy
,
Patrizia TarugiDepartment of Biomedical Sciences, University of Modena and Reggio Emilia, Modena, Italy
,
Elisa Aggazzotti CavazzaOtolaryngology – Head and Neck Surgery Department, University Hospital of Modena, Modena, ItalyCorrespondence[email protected]
&
Antonio PercesepeMedical Genetics – Department of Mother and Child, University Hospital of Modena, Modena, Italy
 show all
Pages 1-7 | Accepted 06 May 2015, Published online: 12 Aug 2015

References

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  • Lee H, Jen JC, Wang H, Chen Z, Mamsa H, Sabatti C, et al. A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity. Hum Mol Genet. 2006;15:251–8.
  • Hurle B, Ignatova E, Massironi SM, Mashimo T, Rios X, Thalmann I, et al. Non-syndromic vestibular disorder with otoconial agenesis in tilted/mergulhador mice caused by mutations in otopetrin 1. Hum Mol Genet. 2003;12:777–89.
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