De Novo Variants in Eef2 Cause a Neurodevelopmental Disorder with Benign External Hydrocephalus

AuthID
P-015-D9C
12
Author(s)
Olson, AN
·
Yoon, G
·
Nimmo, GAM
·
Gomez, CM
·
Willemsen, MA
·
Millan, F
·
Schneider, A
·
Pfundt, R
·
de Brouwer, APM
·
Dinman, JD
·
de Vries, BBA
Document Type
Article
Year published
2020
Published
in Human Molecular Genetics, ISSN: 0964-6906
Volume: 29, Issue: 24, Pages: 3892-3899
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ISSN: 0964-6906
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