(Q33593504)

28 July 2017

title

Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17 (English)

1 reference

28 July 2017

1 reference

Koch MC

1

1 reference

28 July 2017

Ricker K

2

1 reference

28 July 2017

Otto M

3

1 reference

28 July 2017

Grimm T

4

1 reference

28 July 2017

Hoffman EP

5

1 reference

28 July 2017

Rüdel R

6

1 reference

28 July 2017

Bender K

7

1 reference

28 July 2017

Zoll B

8

1 reference

28 July 2017

Harper PS

9

1 reference

28 July 2017

Lehmann-Horn F

10

1 reference

28 July 2017

publication date

1 September 1991

1 reference

Journal of Medical Genetics

28 July 2017

language of work or name

English

0 references

published in

1 reference

28 July 2017

volume

28

1 reference

28 July 2017

issue

9

1 reference

28 July 2017

page(s)

583-586

1 reference

A third type of periodic paralysis, with normokalemia and favourable response to sodium chloride

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015786

Strategies for multilocus linkage analysis in humans

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015786

Two cases of adynamia episodica hereditaria: In vitro investigation of muscle cell membrane and contraction parameters

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015786

A simple salting out procedure for extracting DNA from human nucleated cells

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015786

Perinatal lethal osteogenesis imperfecta (OI type II): a biochemically heterogeneous disorder usually due to new mutations in the genes for type I collagen

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015786

Adynamia episodica hereditaria: Gamstorp's disease or Eulenburg's paramyotonia?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015786

Membrane changes in cells from myotonia patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015786

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015786

Ryanodine receptor gene is a candidate for predisposition to malignant hyperthermia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015786

Altered gating and conductance of Na+ channels in hyperkalemic periodic paralysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015786

21 June 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683408

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Assignment of the gene for central core disease to chromosome 19

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1683408

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1683408

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.28.9.583

1 reference

28 July 2017

1 reference

28 July 2017

1 reference