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

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

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Citations

22

References

2016

Year

David B. Beck, Megan T. Cho, Francisca Millan, Carin Yates, Mark Hannibal, Bridget O’Connor, Marwan Shinawi, Anne M. Connolly, Darrel Waggoner, Sara Halbach,

Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderGeneticsEnamel DefectsDisease Gene IdentificationTooth DevelopmentCtbp1 MutationMedicineDevelopmental Delay

References

	Year	Citations

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