(Q34622306)

3 August 2017

title

Mutation of a potassium channel-related gene in progressive myoclonic epilepsy (English)

1 reference

3 August 2017

1 reference

3

Julie Désir

1 reference

3 August 2017

8

Marc J Abramowicz

1 reference

3 August 2017

Patrick Van Bogaert

1

1 reference

3 August 2017

Regis Azizieh

2

1 reference

3 August 2017

Alec Aeby

4

1 reference

3 August 2017

Linda De Meirleir

5

1 reference

3 August 2017

Jean-François Laes

6

1 reference

3 August 2017

Florence Christiaens

7

1 reference

3 August 2017

publication date

1 June 2007

1 reference

3 August 2017

1 reference

3 August 2017

volume

61

1 reference

3 August 2017

issue

6

1 reference

3 August 2017

page(s)

579-586

1 reference

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

3 August 2017

cites work

1 reference

Progressive myoclonus epilepsies: specific causes and diagnosis

21 January 2018

1 reference

Progressive myoclonic epilepsy

21 January 2018

1 reference

Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects

21 January 2018

1 reference

Clinical presentations and phenomenology of myoclonus

21 January 2018

1 reference

Neurophysiology of positive and negative myoclonus

21 January 2018

1 reference

Advances in the genetics of progressive myoclonus epilepsy

21 January 2018

1 reference

Recent developments in the quest for myoclonic epilepsy genes.

21 January 2018

1 reference

Classification of the myoclonic epilepsies

21 January 2018

1 reference

Myoclonus: current concepts and recent advances.

21 January 2018

1 reference

Complete sequencing and characterization of 21,243 full-length human cDNAs

21 January 2018

1 reference

Neurological potassium channelopathies

21 January 2018

1 reference

Sequence and structural analysis of BTB domain proteins

21 January 2018

1 reference

A new method for autozygosity mapping using single nucleotide polymorphisms (SNPs) and EXCLUDEAR.

21 January 2018

1 reference

Identification of a human brain-specific gene, calneuron 1, a new member of the calmodulin superfamily

21 January 2018

1 reference

Monogenic idiopathic epilepsies

21 January 2018

1 reference

Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+).

21 January 2018

1 reference

KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum

21 January 2018

1 reference

A perfect message: RNA surveillance and nonsense-mediated decay

21 January 2018

1 reference

Controlling potassium channel activities: Interplay between the membrane and intracellular factors

21 January 2018

1 reference

Structure of a voltage-dependent K+ channel beta subunit

21 January 2018

1 reference

A new human gene KCNRG encoding potassium channel regulating protein is a cancer suppressor gene candidate located in 13q14.3.

21 January 2018

1 reference

A tumor necrosis factor alpha- and interleukin 6-inducible protein that interacts with the small subunit of DNA polymerase delta and proliferating cell nuclear antigen

21 January 2018

1 reference

A novel PDIP1-related protein, KCTD10, that interacts with proliferating cell nuclear antigen and DNA polymerase delta

21 January 2018

1 reference

REN: a novel, developmentally regulated gene that promotes neural cell differentiation

21 January 2018

1 reference

Hedgehog antagonist REN(KCTD11) regulates proliferation and apoptosis of developing granule cell progenitors

21 January 2018

1 reference

Isolation from cochlea of a novel human intronless gene with predominant fetal expression

21 January 2018

1 reference

Directional asymmetry of the zebrafish epithalamus guides dorsoventral innervation of the midbrain target

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.21121

1 reference

3 August 2017

1 reference