(Q47827075)

6 February 2018

title

Congenital myasthenic syndromes. Studies of the AChR and other candidate genes. (English)

1 reference

6 February 2018

author name string

Beeson D

1

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6 February 2018

Newland C

2

1 reference

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Croxen R

3

1 reference

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Buckel A

4

1 reference

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Li FY

5

1 reference

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Larsson C

6

1 reference

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Tariq M

7

1 reference

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Vincent A

8

1 reference

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Newsom-Davis J

9

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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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volume

841

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page(s)

181-183

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6 February 2018

Mutations in different functional domains of the human muscle acetylcholine receptor alpha subunit in patients with the slow-channel congenital myasthenic syndrome

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1998.TB10924.X

Crossref

reference URL

retrieved

21 January 2018

Mutation of the acetylcholine receptor alpha subunit causes a slow-channel myasthenic syndrome by enhancing agonist binding affinity

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1998.TB10924.X

Crossref

reference URL

retrieved

21 January 2018

Primary structure of the human muscle acetylcholine receptor. cDNA cloning of the gamma and epsilon subunits

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1998.TB10924.X

Crossref

reference URL

retrieved

21 January 2018

Identifiers

DOI

10.1111/J.1749-6632.1998.TB10924.X

1 reference

6 February 2018

PubMed ID

9668236

1 reference

6 February 2018