(Q48686214)

14 February 2018

title

Developmental abnormalities of cortical interneurons precede symptoms onset in a mouse model of Rett syndrome (English)

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4

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author name string

Giulio Srubek Tomassy

series ordinal

1

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Noemi Morello

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2

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Eleonora Calcagno

series ordinal

3

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language of work or name

English

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publication date

5 August 2014

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14 February 2018

Journal of Neurochemistry

published in

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volume

131

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issue

1

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page(s)

115-127

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

cites work

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MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions

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Three groups of interneurons account for nearly 100% of neocortical GABAergic neurons

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Loss of MeCP2 function is associated with distinct gene expression changes in the striatum

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Identifiers

DOI

10.1111/JNC.12803

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14 February 2018

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14 February 2018