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Haploinsufficiency of PHF21A due to frameshift and nonsense mutations causes syndromic autism including intellectual disability, craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems

Kim, H.; Rosenfeld, J. A.; Scott, D. A.; Benedicte, G.; Labonne, J. D.; Brown, J.; McGuire, M.; Mahida, S.; Naidu, S.; Gutierrez, J., et al.

ArticleIssue Date2019CitationEuropean Journal of Human Genetics, v.27, pp 1394 - 1394PublisherNatue Publishing Group
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