Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22
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A contiguous Not I restriction map of band q22.3 of human chromosome 21Localization of a gene for partial epilepsy to chromosome 10qFamilial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16Analysis of chromosome 21 yeast artificial chromosome (YAC) clonesLong-distance restriction mapping of the proximal long arm of human chromosome 21 with Not I linking clones.Isolation, characterization, and regional mapping of microclones from a human chromosome 21 microdissection libraryGenetics of childhood epilepsyGenetic epilepsy model derived from common inbred mouse strains.Advances in the genetics of progressive myoclonus epilepsy.High-resolution mapping and transcript identification at the progressive epilepsy with mental retardation locus on chromosome 8p.Random-breakage mapping method applied to human DNA sequences.Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.Molecular background of progressive myoclonus epilepsy.A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and ageGenetics of inherited human epilepsiesSegregation analysis of cryptogenic epilepsy and an empirical test of the validity of the results.Genetic analysis of kifafa, a complex familial seizure disorder.Development of a novel rat mutant with spontaneous limbic-like seizures.Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q.Evaluating candidate genes in common epilepsies and the nature of evidenceMolecular background of EPM1-Unverricht-Lundborg disease.Unverricht-Lundborg disease, a condition with self-limited progression: long-term follow-up of 20 patients.Substantial thalamostriatal dopaminergic defect in Unverricht-Lundborg disease.Inherited epilepsies of childhood.Searching for human epilepsy genes: a progress report.Progress in mapping human epilepsy genes.Messages from an isolate: lessons from the Finnish gene pool.Confirmation of linkage in X-linked infantile spasms (West syndrome) and refinement of the disease locus to Xp21.3-Xp22.1.Clinical features and genetics of progressive myoclonus epilepsy of the Univerricht-Lundborg type.Perampanel in 12 patients with Unverricht-Lundborg disease.An interstitial deletion of the long arm of chromosome 21 in a case of a first episode of psychosis.Genetic and developmental influences on susceptibility to epilepsy: evidence from twins.Correction of a Splicing Mutation Affecting an Unverricht-Lundborg Disease Patient by Antisense Therapy
P2860
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P2860
Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
@tr
scientific article published on May 1991
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22
@en
Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22.
@nl
type
label
Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22
@en
Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22.
@nl
prefLabel
Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22
@en
Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22.
@nl
P2093
P2860
P356
P1476
Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22
@en
P2093
Hästbacka J
Koskiniemi M
Lehesjoki AE
Sistonen P
de la Chapelle A
P2860
P304
P356
10.1073/PNAS.88.9.3696
P407
P577
1991-05-01T00:00:00Z