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Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephaly

Title:	Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephaly
Authors:	Herbst, Charlotte^Aff1; Bothe, Viktoria^Aff1; Wegler, Meret^Aff1; Axer-Schaefer, Susanne^Aff2; Audebert-Bellanger, Séverine^Aff3; Gecz, Jozef^Aff4; Cogne, Benjamin^{Aff5, Aff6}; Feldman, Hagit Baris^{Aff7, Aff8}; Horn, Anselm H. C.^{Aff10, Aff9}; Hurst, Anna C. E.^Aff11; Kelly, Melissa A.^Aff12; Kruer, Michael C.^Aff13; Kurolap, Alina^Aff7; Laquerriere, Annie^Aff14; Li, Megan^Aff15; Mark, Paul R.^Aff16; Morawski, Markus^Aff17; Nizon, Mathilde^{Aff5, Aff6}; Pastinen, Tomi^{Aff18, Aff19}; Polster, Tilman^Aff2; Saugier-Veber, Pascale^Aff20; SeSong, Jang^Aff21; Sticht, Heinrich^Aff9; Stieler, Jens T.^Aff17; Thifffault, Isabelle^{Aff18, Aff19}; van Eyk, Clare L.^Aff4; Marcorelles, Pascale^Aff22; Vezain-Mouchard, Myriam^Aff20; Abou Jamra, Rami^Aff1; Oppermann, Henry^{Aff1, IDs00439024026554_cor30}
Source:	Human Genetics. 143(3):455-469
Database:	Springer Nature Journals