Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms. (Q40934865)

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8 March 2020

title

Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms (English)

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8 March 2020

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Charlotte Kilstrup-Nielsen

8 March 2020

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Nicoletta Landsberger

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author name string

Clementina Cobolli Gigli

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Riccardo Lorenzo Rossi

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Linda Scaramuzza

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8 March 2020

publication date

15 May 2015

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8 March 2020

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volume

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issue

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page(s)

2517-2529

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

8 March 2020

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21 January 2018

Identifiers

DOI

10.1093/CERCOR/BHV078

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25979088%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

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