(Q47827062)

6 February 2018

title

Congenital myasthenic syndrome caused by novel loss-of-function mutations in the human AChR epsilon subunit gene. (English)

1 reference

6 February 2018

congenital myasthenic syndrome

main subject

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2

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author name string

M Milone

1

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6 February 2018

T Fukudome

3

1 reference

6 February 2018

X M Shen

4

1 reference

6 February 2018

J Brengman

5

1 reference

6 February 2018

R C Griggs

6

1 reference

6 February 2018

A G Engel

7

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6 February 2018

language of work or name

English

0 references

publication date

1 May 1998

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6 February 2018

Annals of the New York Academy of Sciences

published in

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6 February 2018

volume

841

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6 February 2018

page(s)

184-188

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6 February 2018

End-plate acetylcholine receptor deficiency due to nonsense mutations in the epsilon subunit

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1998.TB10925.X

Acetylcholine receptor epsilon-subunit deletion causes muscle weakness and atrophy in juvenile and adult mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1998.TB10925.X

Relation between subsynaptic receptor blockade and response to quantal transmitter at the mouse neuromuscular junction

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1998.TB10925.X

Toward a structural basis for the function of nicotinic acetylcholine receptors and their cousins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1998.TB10925.X

10.1111/J.1749-6632.1998.TB10925.X

21 January 2018

Identifiers

DOI

1 reference

6 February 2018

PubMed ID

9668237

1 reference

6 February 2018