(Q36870292)

16 August 2017

Prevalence study of genetically defined skeletal muscle channelopathies in England (English)

1 reference

16 August 2017

11

Michael G Hanna

1 reference

16 August 2017

Alejandro Horga

1

1 reference

16 August 2017

Dipa L Raja Rayan

2

1 reference

16 August 2017

Emma Matthews

3

1 reference

16 August 2017

Richa Sud

4

1 reference

16 August 2017

Doreen Fialho

5

1 reference

16 August 2017

Siobhan C M Durran

6

1 reference

16 August 2017

James A Burge

7

1 reference

16 August 2017

Simona Portaro

8

1 reference

16 August 2017

Mary B Davis

9

1 reference

16 August 2017

Andrea Haworth

10

1 reference

16 August 2017

language of work or name

English

0 references

publication date

20 March 2013

1 reference

16 August 2017

1 reference

16 August 2017

80

1 reference

16 August 2017

16

1 reference

16 August 2017

1472-1475

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3662361

16 August 2017

1 reference

Human skeletal muscle sodium channelopathies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3662361

Correlating phenotype and genotype in the periodic paralyses

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3662361

Andersen-Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneity

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3662361

Founder mutations and the high prevalence of myotonia congenita in northern Finland

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3662361

Myotonia congenita in northern Finland: an epidemiological and genetic study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3662361

Molecular and genetic characterisation of German families with paramyotonia congenita and demonstration of founder effect in the Ravensberg families

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3662361

Hyperkalemic periodic paralysis: rapid molecular diagnosis and relationship of genotype to phenotype in 12 families

29 September 2017

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23516313

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23516313

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern Scandinavia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23516313

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1212/WNL.0B013E31828CF8D0

1 reference

16 August 2017

1 reference

16 August 2017

PubMed publication ID

23516313

1 reference