(Q59698070)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16273391%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

title

Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation (English)

1 reference

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8 January 2020

6

1 reference

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8 January 2020

Jurgen Del Favero

8

1 reference

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8 January 2020

Kristl G Claeys

3

0 references

Christine Van Broeckhoven

9

object named as

Christine Van Broeckhoven

1 reference

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8 January 2020

author name string

Liesbet Deprez

1

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8 January 2020

Dominique Audenaert

4

1 reference

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8 January 2020

Tine Van Dyck

5

1 reference

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8 January 2020

Wim Van Paesschen

7

1 reference

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8 January 2020

Peter De Jonghe

10

1 reference

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8 January 2020

Lieve R F Claes

2

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8 January 2020

publication date

5 November 2005

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8 January 2020

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8 January 2020

volume

118

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8 January 2020

issue

5

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8 January 2020

page(s)

618-625

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https://scigraph.springernature.com/pub.10.1007/s00439-005-0077-x

8 January 2020

exact match

0 references

cites work

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

1 reference

12 December 2020

Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21

1 reference

12 December 2020

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.

1 reference

12 December 2020

A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures

1 reference

12 December 2020

Descriptive epidemiology of epilepsy: contributions of population-based studies from Rochester, Minnesota

1 reference

12 December 2020

Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations

1 reference

12 December 2020

Computer-simulation methods in human linkage analysis

1 reference

12 December 2020

Vlgr1 knockout mice show audiogenic seizure susceptibility.

1 reference

12 December 2020

dbSNP: the NCBI database of genetic variation

1 reference

12 December 2020

Novel locus on chromosome 12q22-q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures

1 reference

12 December 2020

SNPbox: a modular software package for large-scale primer design

1 reference

12 December 2020

Faster sequential genetic linkage computations

1 reference

12 December 2020

Very large G protein-coupled receptor-1, the largest known cell surface protein, is highly expressed in the developing central nervous system

1 reference

12 December 2020

Pedigree analysis in families with febrile seizures

1 reference

12 December 2020

A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE Task Force on Classification and Terminology

1 reference

12 December 2020

Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta

1 reference

12 December 2020

First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene

1 reference

12 December 2020

Complex segregation analysis of febrile convulsions

1 reference

12 December 2020

Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest

1 reference

12 December 2020

Generalized epilepsy with febrile seizures plus: A common childhood-onset genetic epilepsy syndrome

1 reference

12 December 2020

Genetic studies of febrile convulsions: analysis of twin and family data

1 reference

12 December 2020

A locus for simple pure febrile seizures maps to chromosome 6q22-q24.

1 reference

12 December 2020

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

1 reference

12 December 2020

A locus for febrile seizures (FEB3) maps to chromosome 2q23-24

1 reference

12 December 2020

Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures

1 reference

12 December 2020

Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes

1 reference

12 December 2020

Significant evidence for linkage of febrile seizures to chromosome 5q14-q15.

1 reference

12 December 2020

Hereditary febrile seizures: phenotype and evidence for a chromosome 19p locus.

1 reference

12 December 2020

Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II

1 reference

12 December 2020

A novel gene causing a mendelian audiogenic mouse epilepsy

1 reference

12 December 2020

10.1007/S00439-005-0077-X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16273391%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

1 reference