Published in
Springer (part of Springer Nature), neurogenetics
DOI: 10.1007/s10048-016-0482-4
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A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects
Journal article published in 2016 by
David B. Beck,
Megan T. Cho,
Francisca Millan,
Carin Yates,
Mark Hannibal,
Bridget O’Connor,
Marwan Shinawi 
,
Anne M. Connolly,
Darrel Waggoner,
Sara Halbach,
Brad Angle,
Victoria Sanders,
Yufeng Shen,
Kyle Retterer,
Amber Begtrup
and other authors.
,
Anne M. Connolly,
Darrel Waggoner,
Sara Halbach,
Brad Angle,
Victoria Sanders,
Yufeng Shen,
Kyle Retterer,
Amber Begtrup
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
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