LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z-) agrin. (Q36696606)

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19 January 2020

title

LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z-) agrin (English)

1 reference

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congenital myasthenic syndrome

19 January 2020

main subject

congenital disorder

0 references

1 reference

based on heuristic

inferred from title

author

Vladimir Yarov-Yarovoy

10

1 reference

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19 January 2020

author name string

Ricardo A Maselli

1

1 reference

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19 January 2020

Jose M Fernandez

2

1 reference

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19 January 2020

Juan Arredondo

3

1 reference

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19 January 2020

Carmen Navarro

4

1 reference

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19 January 2020

Maian Ngo

5

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19 January 2020

David Beeson

6

1 reference

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19 January 2020

Orla Cagney

7

1 reference

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19 January 2020

D Colette Williams

8

1 reference

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19 January 2020

Robert L Wollmann

9

1 reference

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19 January 2020

Michael J Ferns

11

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19 January 2020

publication date

29 December 2011

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19 January 2020

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19 January 2020

volume

131

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19 January 2020

issue

7

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19 January 2020

page(s)

1123-1135

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describes a project that uses

19 January 2020

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4795461/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

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5 September 2018

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5 September 2018

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5 September 2018

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Synaptic transmission is impaired at neuronal autonomic synapses in agrin-null mice

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22205389

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00439-011-1132-4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22205389%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22205389%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

PubMed publication ID

22205389

1 reference