Published in
Wiley Open Access, Molecular Genetics and Genomic Medicine, 11(8), 2020
DOI: 10.1002/mgg3.1481
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A novel UBE3A sequence variant identified in eight related individuals with neurodevelopmental delay, results in a phenotype which does not match the clinical criteria of Angelman syndrome
Journal article published in 2020 by
Amber Geerts‐Haages,
Stijn N. V. Bossuyt,
Inge Besten,
Hennie Bruggenwirth,
Ineke Burgt,
Helger G. Yntema,
A. Mattijs Punt,
Alice Brooks,
Ype Elgersma,
Ben Distel 
,
Marlies Valstar
,
Marlies Valstar
This paper is made freely available by the publisher.
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