TY - JOUR
T1 - CHD2
T2 - One Gene, Many Roles
AU - Nieto-Estevez, Vanesa
AU - Hsieh, Jenny
N1 - Funding Information:
Work in the laboratory is supported by R01NS093992 and R01NS089770 from the NIH . V.N.-E. is supported by a grant from the Lennox-Gastaut Syndrome Foundation . J.H. is supported by the Semmes Foundation, Inc. and the Robert J. Kleberg, Jr. and Helen C. Kleberg Foundation .
Publisher Copyright:
© 2018
PY - 2018/12/5
Y1 - 2018/12/5
N2 - Mutations in the chromodomain helicase DNA-binding 2 (CHD2) gene have been found in patients with a range of neurodevelopmental disorders. In this issue of Neuron, Kim et al. (2018) showed that Chd2 haploinsufficiency compromises cortical development, synaptic function, and memory in mice. Mutations in the chromodomain helicase DNA-binding 2 (CHD2) gene have been found in patients with a range of neurodevelopmental disorders. In this issue of Neuron, Kim et al. (2018) showed that Chd2 haploinsufficiency compromises cortical development, synaptic function, and memory in mice.
AB - Mutations in the chromodomain helicase DNA-binding 2 (CHD2) gene have been found in patients with a range of neurodevelopmental disorders. In this issue of Neuron, Kim et al. (2018) showed that Chd2 haploinsufficiency compromises cortical development, synaptic function, and memory in mice. Mutations in the chromodomain helicase DNA-binding 2 (CHD2) gene have been found in patients with a range of neurodevelopmental disorders. In this issue of Neuron, Kim et al. (2018) showed that Chd2 haploinsufficiency compromises cortical development, synaptic function, and memory in mice.
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U2 - 10.1016/j.neuron.2018.11.036
DO - 10.1016/j.neuron.2018.11.036
M3 - Short survey
C2 - 30521773
AN - SCOPUS:85057224829
SN - 0896-6273
VL - 100
SP - 1014
EP - 1016
JO - Neuron
JF - Neuron
IS - 5
ER -