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English
Epilepsies with single gene inheritance.
scientific article published on January 1997
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scholarly article
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stated in
Europe PubMed Central
PubMed publication ID
9071484
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9071484%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
review article
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Europe PubMed Central
title
Epilepsies with single gene inheritance
(English)
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Europe PubMed Central
PubMed publication ID
9071484
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9071484%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
author
Samuel Berkovic
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9071484
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9071484%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
author name string
I E Scheffer
series ordinal
2
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Europe PubMed Central
PubMed publication ID
9071484
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9071484%20AND%20SRC:MED&resulttype=core&format=json
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1 November 2019
language of work or name
English
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publication date
1 January 1997
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stated in
Europe PubMed Central
PubMed publication ID
9071484
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9071484%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
published in
Brain and Development
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stated in
Europe PubMed Central
PubMed publication ID
9071484
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9071484%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
volume
19
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9071484
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9071484%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9071484
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9071484%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
page(s)
13-18
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9071484
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9071484%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
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Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical Development
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Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene.
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Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20.
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Seizure characteristics in chromosome 20 benign familial neonatal convulsions
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Benign familial neonatal convulsions: confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8q
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Benign infantile familial convulsions
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Benign familial infantile epilepsy
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Benign infantile familial convulsions are not an allelic form of the benign familial neonatal convulsions gene
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EVIDENCE FOR A GENETIC ETIOLOGY OF TEMPORAL-CENTRAL ABNORMALITIES IN FOCAL EPILEPSY.
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Benign epilepsy of childhood with centrotemporal EEG foci: a genetic study
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Benign partial epilepsy and related conditions: multifactorial pathogenesis with hereditary impairment of brain maturation
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Benign occipital epilepsy: a family study
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Reading epilepsy. An appraisal of 20 patients diagnosed at the Mayo Clinic, Rochester, Minnesota, between 1949 and 1989, and delineation of the epileptic syndrome
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Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder
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Genetic linkage studies in familial frontal epilepsy: Exclusion of the human chromosome regions homologous to the El-1 mouse locus
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Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2
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7 January 2021
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Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation
1 reference
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7 January 2021
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The gene for progressive myoclonus epilepsy of the Lafora type maps to chromosome 6q.
1 reference
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Crossref
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Isolation of a novel gene underlying batten disease, CLN3
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Crossref
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7 January 2021
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Identifiers
DOI
10.1016/S0387-7604(96)00060-5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9071484
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9071484%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
PubMed publication ID
9071484
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9071484
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9071484%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
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