Periodic paralysis in quarter horses: a sodium channel mutation disseminated by selective breeding (Q67510312)

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14 September 2019

title

Periodic paralysis in quarter horses: a sodium channel mutation disseminated by selective breeding (English)

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14 September 2019

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Rudolph JA

1

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14 September 2019

Spier SJ

2

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14 September 2019

Byrns G

3

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14 September 2019

Rojas CV

4

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14 September 2019

Bernoco D

5

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14 September 2019

Hoffman EP

6

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14 September 2019

publication date

1 October 1992

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14 September 2019

language of work or name

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14 September 2019

volume

2

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14 September 2019

issue

2

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14 September 2019

page(s)

144-147

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Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene

14 September 2019

cites work

1 reference

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7 January 2021

Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17.

1 reference

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7 January 2021

A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1038%2FNG1092-144

7 January 2021

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1038%2FNG1092-144

7 January 2021

Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita

1 reference

https://api.crossref.org/works/10.1038%2FNG1092-144

7 January 2021

Temperature-sensitive mutations in the III–IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita

1 reference

https://api.crossref.org/works/10.1038%2FNG1092-144

7 January 2021

Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pH

1 reference

https://api.crossref.org/works/10.1038%2FNG1092-144

7 January 2021

Altered ionic permeability in skeletal muscle from horses with hyperkalemic periodic paralysis.

1 reference

https://api.crossref.org/works/10.1038%2FNG1092-144

7 January 2021

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG1092-144

7 January 2021

Primary structure and functional expression of a mammalian skeletal muscle sodium channel

1 reference

https://api.crossref.org/works/10.1038%2FNG1092-144

7 January 2021

Sequence and genomic structure of the human adult skeletal muscle sodium channel alpha subunit gene on 17q

1 reference

https://api.crossref.org/works/10.1038%2FNG1092-144

7 January 2021

A sodium channel defect in hyperkalemic periodic paralysis: potassium-induced failure of inactivation

1 reference

https://api.crossref.org/works/10.1038%2FNG1092-144

7 January 2021

Inactivation of the sodium channel. I. Sodium current experiments

1 reference

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7 January 2021

Dystrophin and disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1092-144

7 January 2021

Construction and comparison of chromosome 21 radiation hybrid and linkage maps using CRI-MAP

1 reference

https://api.crossref.org/works/10.1038%2FNG1092-144

7 January 2021

Primary structure and expression of a sodium channel characteristic of denervated and immature rat skeletal muscle

1 reference

https://api.crossref.org/works/10.1038%2FNG1092-144

7 January 2021

Primary structure of Electrophorus electricus sodium channel deduced from cDNA sequence

1 reference

https://api.crossref.org/works/10.1038%2FNG1092-144

7 January 2021

Identifiers

DOI

10.1038/NG1092-144

1 reference

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14 September 2019

1 reference