Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: Evidence for a third EKD gene (Q57243929)

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12 November 2019

title

Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene (English)

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12 November 2019

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12 November 2019

Thomas Warner

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12 November 2019

Nicholas W. Wood

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Anthony H V Schapira

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Kailash Phatechand Bhatia

12 November 2019

9

object named as

Kailash P Bhatia

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12 November 2019

author name string

Sian D Spacey

1

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12 November 2019

Gurusidheshwar M Wali

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12 November 2019

Paul R Jarman

5

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12 November 2019

Peter H Dixon

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12 November 2019

Mary B Davis

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12 November 2019

language of work or name

English

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publication date

1 July 2002

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12 November 2019

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12 November 2019

volume

17

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page(s)

717-725

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issue

4

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Paroxysmal kinesigenic choreoathetosis: a report of 26 patients

12 November 2019

cites work

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Familial paroxysmal kinesigenic choreoathetosis: an electrophysiologic and genotypic analysis.

21 January 2018

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

21 January 2018

1 reference

Paroxysmal kinesigenic choreoathetosis in Singapore and its relationship to epilepsy.

21 January 2018

1 reference

Epilepsy or paroxysmal kinesigenic choreoathetosis?

21 January 2018

1 reference

An uncommon seizure disorder: familial paroxysmal choreoathetosis

21 January 2018

1 reference

Seizure induced by movement

21 January 2018

1 reference

Paroxysmal dyskinesias: clinical features and classification

21 January 2018

1 reference

Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16

21 January 2018

1 reference

Association of infantile convulsions with paroxysmal dyskinesias (ICCA syndrome): confirmation of linkage to human chromosome 16p12-q12 in a Chinese family

21 January 2018

1 reference

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

21 January 2018

1 reference

Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies

21 January 2018

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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.

21 January 2018

1 reference

Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2.

21 January 2018

1 reference

Ion channels and neurological disease: DNA based diagnosis is now possible, and ion channels may be important in common paroxysmal disorders

21 January 2018

1 reference

A comprehensive genetic map of the human genome based on 5,264 microsatellites

21 January 2018

1 reference

A potassium channel mutation in neonatal human epilepsy

21 January 2018

1 reference

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

21 January 2018

1 reference

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

21 January 2018

1 reference

An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy

21 January 2018

1 reference

Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16q

21 January 2018

1 reference

Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity.

21 January 2018

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Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution

21 January 2018

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Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a "hot spot" for recombination at 16p12.

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/MDS.10126

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12 November 2019

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