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Mutation-specific pathophysiological mechanisms in a new SATB1 -associated neurodevelopmental disorder
Mutation-specific pathophysiological mechanisms in a new SATB1 -associated neurodevelopmental disorder
2020
Joery den Hoed
E de Boer
N Voisin
N. Guex
Lot Snijders Blok
J. Chrast
Linda Manwaring
Marcia C. Willing
A Waheeb
M. Osmond
K. McWalter
Antonio Vitobello
Florence Demurger
A Lavillaureix
S. Odent
B. Mazel
Laurence Faivre
I Thiffault
C. Schwager
S. M. Amudhavalli
Jill A. Rosenfeld
K Radtke
E Preiksaitiene
E. Ranza
Christel Depienne
A. Kuechler
S. Mohammed
Y. Hamzavi Abedi
V.R. Bonagura
B Zuccarelli
B Horist
V. Krishnamurthy
A. A. Kattentidt-Mouravieva
L. Granger
A. Petersen
K. L. Jones
M. Sinnema
Alexander P. A. Stegmann
R Newbury-Ecob
U. Kini
Dianne F. Newbury
Christian Gilissen
H.G. Brunner
Tjitske Kleefstra
A. Reymond
L. E. L. M. Vissers
Simon E. Fisher
Keywords:
Neurodevelopmental disorder
SATB1
Neuroscience
Pathophysiology
Mutation
Medicine
Correction
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