Cite
HARVARD Citation
Millan, F. et al. (2016). Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder. American journal of medical genetics. 170 (7), pp. 1791-1798. [Online].
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Millan, F. et al. (2016). Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder. American journal of medical genetics. 170 (7), pp. 1791-1798. [Online].