Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval

scientific article published on June 1995

Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval is …
instance of (P31):
scholarly articleQ13442814

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P932PMC publication ID1801081
P698PubMed publication ID7762565

P2093author name stringRichard I
Broux O
Chiannilkulchai N
Fougerousse F
Pereira de Souza A
Brenguier L
Allamand V
Bourg N
Devaud C
Pasturaud P
P2860cites workMutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2AQ24314667
The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mappingQ24321747
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian familiesQ24514983
Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22Q28242301
A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2pQ28243860
Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mappingQ28249374
Population frequencies of inherited neuromuscular diseases—A world surveyQ28266298
Identification of the cystic fibrosis gene: genetic analysisQ29614402
Homozygosity mapping: a way to map human recessive traits with the DNA of inbred childrenQ29615807
Multilocus linkage analysis in humans: detection of linkage and estimation of recombinationQ29620848
A second-generation linkage map of the human genomeQ33192755
A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene.Q34302048
Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mappingQ34345703
Molecular analysis of Hurler syndrome in Druze and Muslim Arab patients in Israel: multiple allelic mutations of the IDUA gene in a small geographic areaQ35194898
Linkage disequilibria between pairs of loci within a highly polymorphic region of chromosome 2Q.Q35198651
Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypesQ35199415
Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellitesQ35888843
Recombinations in individuals homozygous by descent localize the Friedreich ataxia locus in a cloned 450-kb interval.Q35889199
Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region.Q35889324
Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1).Q35889622
Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy.Q36731351
Multiple mutations are responsible for the high frequency of metachromatic leukodystrophy in a small geographic areaQ41762644
Consanguinity in a midwestern United States isolateQ42040466
Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15.Q54774379
Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in FinlandQ55671005
Genetic heterogeneity of autosomal recessive limbgirdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusQ57398301
Targeted Development of Microsatellite Markers from Inter-Alu Amplification of YAC ClonesQ57398318
A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellitesQ57398320
Mapping of two chromosome 15 microsatellitesQ57398354
Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical diseaseQ59242124
A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkageQ63979954
Limb-girdle syndrome: a genetic study of 22 large Brazilian families comparison with X-linked Duchenne and Becker dystrophiesQ67932796
A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)Q72202059
Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2Q72635328
P433issue6
P407language of work or nameEnglishQ1860
P921main subjectlimb-girdle muscular dystrophyQ1531322
P304page(s)1417-1430
P577publication date1995-06-01
P1433published inAmerican Journal of Human GeneticsQ4744249
P1476titlePreferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval
P478volume56

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cites work (P2860)
Q48070100An STS map of the limb girdle muscular dystrophy type 2A region.
Q42036972Calpainopathy-a survey of mutations and polymorphisms
Q24678754DNA studies of limb-girdle muscular dystrophy type 2A in the Amish exclude a modifying mitochondrial gene and show no evidence for a modifying nuclear gene
Q34043760Genetic and physical mapping of the locus for autosomal dominant renal Fanconi syndrome, on chromosome 15q15.3.
Q56459995Klinik und Genetik der Gliederg�rteldystrophien
Q35882131Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype.
Q34385428Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3.
Q24680877Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins
Q42588732Multiple mutations in a specific gene in a small geographic area: a common phenomenon?
Q35954589Predicting the range of linkage disequilibrium
Q24530091Recombinant expression and isolation of human L-arginine:glycine amidinotransferase and identification of its active-site cysteine residue
Q42589339The Réunion paradox and the digenic model

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