A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects

Overview of attention for article published in neurogenetics, April 2016

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PubMed: A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth… https://t.co/ycszJmaBjU

Pubmed: A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth… https://t.co/kWjMjzg4rZ

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