Published in
Cell Press, American Journal of Human Genetics, 2(108), p. 346-356, 2021
DOI: 10.1016/j.ajhg.2021.01.007
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Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction
Journal article published in 2021 by
Joery den Hoed,
Elke de Boer,
Norine Voisin,
Alexander Jm M. Dingemans,
Nicolas Guex 
,
Laurens Wiel ,
Christoffer Nellaker,
Emmanuèlle C. Délot,
Florence Démurger,
Shivarajan M. Amudhavalli,
Christel Depienne,
Siddharth Banka,
Dian Donnai,
Y. Hamzavi Abedi,
David A. Dyment
and other authors.
,
Laurens Wiel ,
Christoffer Nellaker,
Emmanuèlle C. Délot,
Florence Démurger,
Shivarajan M. Amudhavalli,
Christel Depienne,
Siddharth Banka,
Dian Donnai,
Y. Hamzavi Abedi,
David A. Dyment
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
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