(Q34146445)

31 July 2017

title

Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5. (English)

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juvenile myoclonic epilepsy

31 July 2017

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Toshimitsu Suzuki

1

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31 July 2017

Ryoji Morita

2

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31 July 2017

Yoshihisa Sugimoto

3

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31 July 2017

Takashi Sugawara

4

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31 July 2017

Dong-Sheng Bai

5

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31 July 2017

Maria E Alonso

6

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31 July 2017

Marco T Medina

7

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31 July 2017

Julia N Bailey

8

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31 July 2017

Astrid Rasmussen

9

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31 July 2017

Jaime Ramos-Peek

10

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31 July 2017

Sergio Cordova

11

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31 July 2017

Francisco Rubio-Donnadieu

12

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31 July 2017

Adriana Ochoa

13

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31 July 2017

Aurelio Jara-Prado

14

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31 July 2017

Johji Inazawa

15

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31 July 2017

Antonio V Delgado-Escueta

16

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31 July 2017

Kazuhiro Yamakawa

17

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31 July 2017

publication date

1 August 2002

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31 July 2017

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31 July 2017

volume

50

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31 July 2017

issue

3

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31 July 2017

page(s)

265-275

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Identification of a novel member of the chloride intracellular channel gene family (CLIC5) that associates with the actin cytoskeleton of placental microvilli

31 July 2017

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

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7 January 2021

Juvenile myoclonic epilepsy of Janz.

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7 January 2021

Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients

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7 January 2021

Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q.

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https://api.crossref.org/works/10.1016%2FS0920-1211%2802%2900052-9

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0920-1211%2802%2900052-9

7 January 2021

Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6

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https://api.crossref.org/works/10.1016%2FS0920-1211%2802%2900052-9

7 January 2021

Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsy

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https://api.crossref.org/works/10.1016%2FS0920-1211%2802%2900052-9

7 January 2021

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

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https://api.crossref.org/works/10.1016%2FS0920-1211%2802%2900052-9

7 January 2021

Juvenile myoclonic epilepsy in chromosome 6p12-p11: locus heterogeneity and recombinations

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7 January 2021

Exclusion of the JRK/JH8 gene as a candidate for human childhood absence epilepsy mapped on 8q24.

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7 January 2021

slit: an extracellular protein necessary for development of midline glia and commissural axon pathways contains both EGF and LRR domains

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7 January 2021

Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.

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7 January 2021

Clinical and genetic analysis of a large pedigree with juvenile myoclonic epilepsy.

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7 January 2021

SUR-8, a conserved Ras-binding protein with leucine-rich repeats, positively regulates Ras-mediated signaling in C. elegans

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7 January 2021

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

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7 January 2021

Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures

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7 January 2021

A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

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https://api.crossref.org/works/10.1016%2FS0920-1211%2802%2900052-9

7 January 2021

A novel gene in the chromosomal region for juvenile myoclonic epilepsy on 6p12 encodes a brain-specific lysosomal membrane protein

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7 January 2021

R-banding and nonisotopic in situ hybridization: precise localization of the human type II collagen gene (COL2A1)

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7 January 2021

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7 January 2021

Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6.

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https://api.crossref.org/works/10.1016%2FS0920-1211%2802%2900052-9

7 January 2021

10.1016/S0920-1211(02)00052-9

Identifiers

DOI

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31 July 2017

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