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Biallelic null variants in ZNF142 cause global developmental delay with familial epilepsy and dysmorphic features

Shinichi Kameyama1,2, Takeshi Mizuguchi1, Hiromi Fukuda1,3

  • 1Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

Journal of Human Genetics
|September 17, 2021
PubMed

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