De novo and biallelic DEAF1 variants cause a phenotypic spectrum.
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Nabais Sá MJ, et al. Among authors: manzini mc.
Genet Med. 2019 Sep;21(9):2059-2069. doi: 10.1038/s41436-019-0473-6. Epub 2019 Mar 29.
Genet Med. 2019.
PMID: 30923367
Free article.