(Q82140254)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16386935%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

title

Mutation screening in Chinese hypokalemic periodic paralysis patients (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16386935%20AND%20SRC:MED&resulttype=core&format=json

hypokalemic periodic paralysis

15 January 2020

main subject

1 reference

Weiqing Wang

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16386935%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Lei Jiang

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16386935%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Lei Ye

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16386935%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Na Zhu

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16386935%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Tingwei Su

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16386935%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Liqing Guan

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16386935%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Xiaoying Li

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16386935%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Guang Ning

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16386935%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

publication date

4 January 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16386935%20AND%20SRC:MED&resulttype=core&format=json

Molecular Genetics and Metabolism

15 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16386935%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

volume

87

1 reference

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15 January 2020

issue

4

1 reference

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15 January 2020

page(s)

359-363

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16386935%20AND%20SRC:MED&resulttype=core&format=json

Hypokalaemia and paralysis

15 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

A calcium channel mutation causing hypokalemic periodic paralysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

Sodium channel inactivation defects are associated with acetazolamide-exacerbated hypokalemic periodic paralysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

A novel sodium channel mutation in a family with hypokalemic periodic paralysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

Temperature-sensitive sodium channelopathy with heat-induced myotonia and cold-induced paralysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

A mutation in the KCNE3 potassium channel gene is associated with susceptibility to thyrotoxic hypokalemic periodic paralysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

No mutation in the KCNE3 potassium channel gene in Chinese thyrotoxic hypokalaemic periodic paralysis patients.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

Mutation screening in Korean hypokalemic periodic paralysis patients: a novel SCN4A Arg672Cys mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

Impairment of skeletal muscle adenosine triphosphate-sensitive K+ channels in patients with hypokalemic periodic paralysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

Skeletal muscle sodium current is reduced in hypokalemic periodic paralysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

Genomic organization of the human skeletal muscle sodium channel gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

Manifestation, management and molecular analysis of candidate genes in two rare cases of thyrotoxic hypokalemic periodic paralysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

Skeletal muscle dihydropyridine-sensitive calcium channel (CACNA1S) gene mutations in chinese patients with hypokalemic periodic paralysis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

Absence of ion channels CACN1AS and SCN4A mutations in thyrotoxic hypokalemic periodic paralysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.10.020

10.1016/J.YMGME.2005.10.020

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16386935%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

1 reference