Published in
Wiley, The American Journal of Medical Genetics - Part A, 5(182), p. 962-973, 2020
DOI: 10.1002/ajmg.a.61505
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De novo heterozygous missense and loss‐of‐function variants in CDC42BPB are associated with a neurodevelopmental phenotype
Journal article published in 2020 by
Ilana Chilton 
,
Volkan Okur,
Giuseppina Vitiello ,
Angelo Selicorni ,
Milena Mariani,
Koen van Gassen,
Alice Goldenberg,
Thomas Husson ,
Dominique Campion,
Klaske D. Lichtenbelt,
Koen Gassen,
Michelle Steinraths,
Jennifer Rice,
Elizabeth R. Roeder,
Rebecca O. Littlejohn
and other authors.
,
Volkan Okur,
Giuseppina Vitiello ,
Angelo Selicorni ,
Milena Mariani,
Koen van Gassen,
Alice Goldenberg,
Thomas Husson ,
Dominique Campion,
Klaske D. Lichtenbelt,
Koen Gassen,
Michelle Steinraths,
Jennifer Rice,
Elizabeth R. Roeder,
Rebecca O. Littlejohn
and other authors.
This paper is made freely available by the publisher.
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