De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies

Fritzen, Daniel; Kuechler, Alma; Grimmel, Mona; Becker, Jessica; Peters, Sophia; Sturm, Marc; Hundertmark, Hela; Schmidt, Axel; Kreiss, Martina; Strom, Tim M.; Wieczorek, Dagmar; Haack, Tobias B.; Beck-Woedl, Stefanie; Cremer, Kirsten; Engels, Hartmut

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De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies

Author:

Fritzen, Daniel; Kuechler, Alma; Grimmel, Mona; Becker, Jessica; Peters, Sophia; Sturm, Marc; Hundertmark, Hela; Schmidt, Axel; Kreiss, Martina; Strom, Tim M.; Wieczorek, Dagmar; Haack, Tobias B.; Beck-Woedl, Stefanie; Cremer, Kirsten; Engels, Hartmut

Tübinger Autor(en):

Grimmel, Mona
Sturm, Marc
Beck-Wödl, Stefanie
Haack, Tobias

Published in:

Human Genetics (2018), Bd. 137, H. 5, S. 401-411

Verlagsangabe:

Springer

Language:

English

Full text:

http://dx.doi.org/10.1007/s00439-018-1892-1

ISSN:

1432-1203