(Q85028767)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21964664%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

title

Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters (English)

1 reference

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13 February 2020

1 reference

Jesse B.G. Hayesmoore

3

1 reference

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13 February 2020

author name string

Victoria Harrison

1

1 reference

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13 February 2020

Lyndsey Connell

2

1 reference

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13 February 2020

Joanna McParland

4

1 reference

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13 February 2020

Michael G Pike

5

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13 February 2020

Edward Blair

6

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13 February 2020

publication date

30 September 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21964664%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics

13 February 2020

published in

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13 February 2020

volume

155A

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13 February 2020

issue

11

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13 February 2020

page(s)

2826-2831

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13 February 2020

Identifiers

DOI

10.1002/AJMG.A.34255

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13 February 2020

1 reference