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Published in 2021 at "Journal of pediatric genetics"
DOI: 10.1055/s-0040-1710330
Abstract: De novo heterozygous mutations in the KAT6A gene give rise to a distinct intellectual disability syndrome, with features including speech delay, cardiac anomalies, craniofacial dysmorphisms, and craniosynostosis. Here, we reported a 16-year-old girl with a…
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Keywords:
mutation kat6a;
kat6a associated;
pancraniosynostosis;
frameshift mutation ... See more keywords