(Q81478314)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17952630%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

title

Localization and mutation detection for paroxysmal kinesigenic choreoathetosis (English)

1 reference

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9 January 2020

1 reference

Te Du

1

1 reference

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9 January 2020

Bin Feng

2

1 reference

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9 January 2020

Xin Wang

3

1 reference

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9 January 2020

Wei Mao

4

1 reference

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9 January 2020

Xilin Zhu

5

1 reference

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9 January 2020

Liping Li

6

1 reference

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9 January 2020

Bei Sun

7

1 reference

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9 January 2020

Nifang Niu

8

1 reference

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9 January 2020

Yang Liu

9

1 reference

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9 January 2020

Yuping Wang

10

1 reference

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9 January 2020

Biao Chen

11

1 reference

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9 January 2020

Xingqiu Cai

12

1 reference

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9 January 2020

Ying Liu

13

1 reference

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9 January 2020

publication date

19 October 2007

1 reference

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Journal of Molecular Neuroscience

9 January 2020

published in

1 reference

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9 January 2020

volume

34

1 reference

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9 January 2020

issue

2

1 reference

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9 January 2020

page(s)

101-107

1 reference

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https://scigraph.springernature.com/pub.10.1007/s12031-007-9012-z

9 January 2020

exact match

0 references

cites work

Molecular cloning, genomic organization, and functional expression of Na+/H+ exchanger isoform 5 (NHE5) from human brain

1 reference

12 December 2020

A cluster of three novel Ca2+ channel gamma subunit genes on chromosome 19q13.4: evolution and expression profile of the gamma subunit gene family

1 reference

12 December 2020

Familial paroxysmal kinesigenic choreoathetosis: an electrophysiologic and genotypic analysis

1 reference

12 December 2020

Multicenter study of paroxysmal dyskinesias in Japan--clinical and pedigree analysis

1 reference

12 December 2020

A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16.

1 reference

12 December 2020

Identification of three novel Ca(2+) channel gamma subunit genes reveals molecular diversification by tandem and chromosome duplication

1 reference

12 December 2020

A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16

1 reference

12 December 2020

Mutation analysis of the sodium/hydrogen exchanger gene (NHE5) in familial paroxysmal kinesigenic dyskinesia

1 reference

12 December 2020

Channelopathy: hypothesis of a common pathophysiologic mechanism in different forms of paroxysmal dyskinesia.

1 reference

12 December 2020

Disorders of membrane channels or channelopathies

1 reference

12 December 2020

Exquisite sensitivity of paroxysmal kinesigenic choreoathetosis to carbamazepine

1 reference

12 December 2020

[Non-epileptic paroxysmal movement disorders]

1 reference

12 December 2020

Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1.

1 reference

12 December 2020

Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: Evidence for a third EKD gene

1 reference

12 December 2020

Two new genes from the human ATP-binding cassette transporter superfamily, ABCC11 and ABCC12, tandemly duplicated on chromosome 16q12.

1 reference

12 December 2020

The relationship between paroxysmal kinesigenic choreoathetosis and epilepsy.

1 reference

12 December 2020

The paroxysmal dyskinesias

1 reference

12 December 2020