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