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Original article
Enrichment of damaging missense variants in genes related with axonal guidance signalling in sporadic Meniere’s disease

Authors

  • Alvaro Gallego-Martinez Otology & Neurotology Group CTS 495, Genomic Medicine Area, Centro de Genomica e Investigación Oncológica, Pfizer-Universidad de Granada-Junta de Andalucía, Granada, Spain Bioinformatics Core, Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-Sur-Alzette, Luxembourg PubMed articlesGoogle scholar articles
  • Teresa Requena Otology & Neurotology Group CTS 495, Genomic Medicine Area, Centro de Genomica e Investigación Oncológica, Pfizer-Universidad de Granada-Junta de Andalucía, Granada, Spain PubMed articlesGoogle scholar articles
  • Pablo Roman-Naranjo Otology & Neurotology Group CTS 495, Genomic Medicine Area, Centro de Genomica e Investigación Oncológica, Pfizer-Universidad de Granada-Junta de Andalucía, Granada, Spain PubMed articlesGoogle scholar articles
  • Patrick May Bioinformatics Core, Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-Sur-Alzette, Luxembourg PubMed articlesGoogle scholar articles
  • Jose A Lopez-Escamez Otology & Neurotology Group CTS 495, Genomic Medicine Area, Centro de Genomica e Investigación Oncológica, Pfizer-Universidad de Granada-Junta de Andalucía, Granada, Spain Department of Otolaryngology, Instituto de Investigación Biosanitaria, ibs.GRANADA, Hospital Universitario Virgen de las Nieves, Granada, Spain PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Jose A Lopez-Escamez, Genome medicine area, Centro Pfizer - Universidad de Granada - Junta de Andalucia de Genomica e Investigacion Oncologica, Granada 18016, Spain; antonio.lopezescamez{at}genyo.es
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Citation

Gallego-Martinez A, Requena T, Roman-Naranjo P, et al
Enrichment of damaging missense variants in genes related with axonal guidance signalling in sporadic Meniere’s disease

Publication history

  • Received March 18, 2019
  • Revised July 17, 2019
  • Accepted August 3, 2019
  • First published September 7, 2019.
Online issue publication 
January 23, 2020

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