DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Millan F, Cho MT, Retterer K. , et al.
Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder.
Am J Med Genet A 2016;
170 (07) 1791-1798
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