Literature DB >> 8743986

Genetic and physical mapping of the progressive epilepsy with mental retardation (EPMR) locus on chromosome 8p.

S Ranta1, A E Lehesjoki, A Hirvasniemi, J Weissenbach, B Ross, S M Leal, A de la Chapelle, T C Gilliam.   

Abstract

Progressive epilepsy with mental retardation (EPMR) is an autosomal recessive disorder discovered recently from an isolated region in Finland. The disorder is characterized by normal early development, generalized tonic-clonic seizures with onset at 5-10 years of age, and progressive mental retardation beginning 2-5 years after the onset of seizures. We recently mapped the EPMR locus to a 7-cM region on chromosome 8p between markers AFM185xb2 and D8S262. A recombination detected with a new microsatellite marker AFMa054td9 narrows the region to 4 cM. A yeast artificial chromosome (YAC) contig containing 22 YACs was constructed across the disease gene region. The YAC contig is characterized by a collection of 19 YAC-end sequence-tag sites together with seven microsatellite markers. The entire YAC contig spans a minimum of 3 Mb. Moreover, the distal end of the contig contains a subtelomeric YAC yRM2205 that anchors the contig to the telomere. Construction of a YAC contig across the disease gene region is an essential step toward the isolation of the EPMR gene.

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Year:  1996        PMID: 8743986      PMCID: PMC6145179          DOI: 10.1101/gr.6.5.351

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  37 in total

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Journal:  N Engl J Med       Date:  1990-11-22       Impact factor: 91.245

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Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

3.  Refinement of the spinal muscular atrophy locus by genetic and physical mapping.

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Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

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Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

5.  Avoiding recomputation in linkage analysis.

Authors:  A A Schäffer; S K Gupta; K Shriram; R W Cottingham
Journal:  Hum Hered       Date:  1994 Jul-Aug       Impact factor: 0.444

Review 6.  The treatable epilepsies. (First of Two Parts).

Authors:  A V Delgado-Escueta; D M Treiman; G O Walsh
Journal:  N Engl J Med       Date:  1983-06-23       Impact factor: 91.245

7.  Mapping, cloning and genetic characterization of the region containing the Wilson disease gene.

Authors:  K Petrukhin; S G Fischer; M Pirastu; R E Tanzi; I Chernov; M Devoto; L M Brzustowicz; E Cayanis; E Vitale; J J Russo
Journal:  Nat Genet       Date:  1993-12       Impact factor: 38.330

8.  Characterization of the cathepsin B gene and multiple mRNAs in human tissues: evidence for alternative splicing of cathepsin B pre-mRNA.

Authors:  Q Gong; S J Chan; A S Bajkowski; D F Steiner; A Frankfater
Journal:  DNA Cell Biol       Date:  1993-05       Impact factor: 3.311

9.  A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.

Authors:  O K Steinlein; J C Mulley; P Propping; R H Wallace; H A Phillips; G R Sutherland; I E Scheffer; S F Berkovic
Journal:  Nat Genet       Date:  1995-10       Impact factor: 38.330

10.  Localization of the squalene synthase gene (FDFT1) to human chromosome 8p22-p23.1.

Authors:  I Shechter; D G Conrad; I Hart; R C Berger; T L McKenzie; J Bleskan; D Patterson
Journal:  Genomics       Date:  1994-03-01       Impact factor: 5.736

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  1 in total

1.  Mutational analysis of the defective protease in classic late-infantile neuronal ceroid lipofuscinosis, a neurodegenerative lysosomal storage disorder.

Authors:  D E Sleat; R M Gin; I Sohar; K Wisniewski; S Sklower-Brooks; R K Pullarkat; D N Palmer; T J Lerner; R M Boustany; P Uldall; A N Siakotos; R J Donnelly; P Lobel
Journal:  Am J Hum Genet       Date:  1999-06       Impact factor: 11.025

  1 in total

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