A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation

Overview of attention for article published in Human Molecular Genetics, January 2015

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A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell… https://t.co/rxXiSTpbff

More papers on the link between dyslexia and cilia: http://t.co/zBUep4OL8g http://t.co/nf4ARbjcIb

A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell… http://t.co/A3AQ3EcpYQ

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