Epilepsy and fragile X gene mutations (Q48870569)

16 February 2018

title

Epilepsy and fragile X gene mutations (English)

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16 February 2018

author name string

Kluger G

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16 February 2018

Böhm I

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16 February 2018

Laub MC

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16 February 2018

Waldenmaier C

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16 February 2018

publication date

1 November 1996

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16 February 2018

published in

Pediatric Neurology

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16 February 2018

volume

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16 February 2018

issue

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16 February 2018

page(s)

358-360

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16 February 2018

Transmitting males and carrier females in fragile X--revisited.

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900251-2

7 January 2021

Epilepsy and fragile X syndrome: a follow-up study

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900251-2

7 January 2021

Fragile X mental retardation: prevalence in a group of institutionalized patients in Italy and description of a novel EEG pattern

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900251-2

7 January 2021

The Fra(X) syndrome: neurological, electrophysiological, and neuropathological abnormalities

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900251-2

7 January 2021

Benign childhood epilepsy with centrotemporal spikes and the focal sharp wave trait is not linked to the fragile X region

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900251-2

7 January 2021

Detection of full fragile X mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900251-2

7 January 2021

Benign partial epilepsy and related conditions: multifactorial pathogenesis with hereditary impairment of brain maturation

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900251-2

7 January 2021

Frequency and stability of the fragile X premutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900251-2

7 January 2021

The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900251-2

7 January 2021

Essential role for KH domains in RNA binding: impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900251-2

7 January 2021

Neuroanatomy of fragile X syndrome: the temporal lobe

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900251-2

7 January 2021

10.1016/S0887-8994(96)00251-2

Identifiers

DOI

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16 February 2018

release_spwpggtumbemtg2w4zk2ruigs4

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/spwpggtumbemtg2w4zk2ruigs4

24 November 2022

mapped directly with Wikidata item

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16 February 2018