(Q50560371)

English

Identification of mutations in the CACNL1A3 gene in 13 families of Scandinavian origin having hypokalemic periodic paralysis and evidence of a founder effect in Danish families.

scientific article published in March 1997

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

Identification of mutations in the CACNL1A3 gene in 13 families of Scandinavian origin having hypokalemic periodic paralysis and evidence of a founder effect in Danish families. (English)

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

hypokalemic periodic paralysis

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Sillén A

1

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

Sørensen T

2

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

Kantola I

3

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

Friis ML

4

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

Gustavson KH

5

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

Wadelius C

6

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

publication date

1 March 1997

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

American Journal of Medical Genetics Part A

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

69

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

1

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

102-106

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970303%2969%3A1%3C102%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

21 January 2018

Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970303%2969%3A1%3C102%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970303%2969%3A1%3C102%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

21 January 2018

Assignment of the human gene for the alpha 1 subunit of the skeletal muscle DHP-sensitive Ca2+ channel (CACNL1A3) to chromosome 1q31-q32

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970303%2969%3A1%3C102%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

21 January 2018

A calcium channel mutation causing hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970303%2969%3A1%3C102%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

21 January 2018

Familial hypokalaemic periodic paralysis in Finland

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970303%2969%3A1%3C102%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

21 January 2018

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970303%2969%3A1%3C102%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

21 January 2018

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970303%2969%3A1%3C102%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

21 January 2018

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970303%2969%3A1%3C102%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970303%2969%3A1%3C102%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

21 January 2018

Recent human germ-line mutation: inferences from patients with hemophilia B.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970303%2969%3A1%3C102%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

21 January 2018

A second-generation linkage map of the human genome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970303%2969%3A1%3C102%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

21 January 2018

Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970303%2969%3A1%3C102%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

21 January 2018

Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970303%2969%3A1%3C102%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

21 January 2018

Identifiers

10.1002/(SICI)1096-8628(19970303)69:1<102::AID-AJMG20>3.0.CO;2-S

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/9066893

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50560371&oldid=1965249837"