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Biallelic Gins2 Variant P.(Arg114Leu) Causes Meier-Gorlin Syndrome with Craniosynostosis
AuthID
P-015-D9E
8
Author(s)
Nabais Sá, MJ
·
Miller, KA
·
McQuaid, M
·
Koelling, N
·
Wilkie, AOM
·
Wurtele, H
·
de Brouwer, APM
·
Oliveira, J
Document Type
Article
Year published
2021
Published
in
Journal of Medical Genetics,
ISSN: 0022-2593
Volume: 59, Issue: 8, Pages: 776-780
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Publication Identifiers
DOI
:
10.1136/jmedgenet-2020-107572
Source Identifiers
ISSN
: 0022-2593
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