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Updated: May 12, 2026

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

Cardiomiopatía dilatada y pérdida auditiva neurosensorial: un síndrome hereditario que se corresponde con 6q23-24

J Schönberger1, H Levy, E Grünig

  • 1Department of Genetics and Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02115, USA.

Circulation
|April 19, 2000
PubMed
Resumen

Un nuevo trastorno genético vincula la pérdida de audición juvenil con la insuficiencia cardíaca en adultos. Este síndrome cardioauditivo, causado por una mutación en el cromosoma 6q23-24, permite la identificación temprana de individuos en riesgo.

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