DOI:
10.1055/s-00044025
Annals of the National Academy of Medical Sciences (India)
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References
Beck DB, Cho MT, Millan F. et al
A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects.
Neurogenetics 2016;
17 (03) 173-178
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