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Widening of the genetic and clinical spectrum of Lamb–Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency
Authors
Akay E
Akilapa R
+83 more
Alembik Y
Bacino CA
Barbaro-Dieber T
Bertoli M
Bhoj EJ
Bijlsma E
Bird LM
Blackburn PR
Bressi R
Bruel A-L
Canham N
Chang RC
Charles P
Cherik F
Clark GD
Clark KJ
Cogne B
Cole T
Depienne C
Dubourg C
Dupuis L
Dupuis-Girod S
El Chehadeh S
Fassi E
Francannet C
Gerkes EH
Goyette A-ME
Guillen Sacoto MJ
Hartmann A
Haseeb A
Hilhorst-Hofstee Y
Hoffer MJV
Ichikawa S
Jaillard S
Joseph M
Karimov C
Keren B
Klee EW
Kuechler A
Lefebvre V
Lehalle D
Lesca G
Levy J
Lindstrom K
Machol K
Marey I
Masser-Frye D
McWalter K
Mendoza-Londono R
Mignot C
Monin P
Moutton S
Nambot S
Narayanan V
Nava C
Nizon M
Odent S
Ortega L
Perrin L
Piton A
Poisson A
Ramsey KM
Rosenfeld JA
Rump P
Russell L
Salter CG
Sanchez Russo R
Schluth-Bolard C
Schnur RE
Scott DA
Sigafoos A
Srour M
Tabet A-C
Thomas RH
Vandersteen A
Vargas M
Wang X
Wassink-Ruiter JSK
Willing M
Wojcik A
Zawerton A
Zhu Z
Zwolinski S
Publication date
1 January 2019
Publisher
Nature Publishing Group
Abstract
Abstract is not available.
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oai:eprints.ncl.ac.uk:261308
Last time updated on 30/05/2021