A novel de novo heterozygous DYRK1A mutation causes...

Scientific Reports 2020 / 12 Vol. 10; Iss. 1

A novel de novo heterozygous DYRK1A mutation causes complete loss of DYRK1A function and developmental delay

Lee, Kyu-Sun, Choi, Miri, Kwon, Dae-Woo, Kim, Doyoun, Choi, Jong-Moon, Kim, Ae-Kyeong, Ham, Youngwook, Han, Sang-Bae, Cho, Sungchan, Cheon, Chong Kun
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Volume:
10
Journal:
Scientific Reports
DOI:
10.1038/s41598-020-66750-y
Date:
December, 2020
File:
PDF, 1.97 MB
2020
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