Normal variation at the myotonic dystrophy locus in global human populations. - Wikidata - awgldk - TriplyDB

Normal variation at the myotonic dystrophy locus in global human populations.

Normal variation at the myotonic dystrophy locus in global human populations.

http://www.wikidata.org/entity/Q41972483

about

High germinal instability of the (CTG)n at the SCA8 locus of both expanded and normal alleles De novo myotonic dystrophy mutation in a Nigerian kindred.Fragile X gene instability: anchoring AGGs and linked microsatellites A sequence variation scan of the coagulation factor VIII (FVIII) structural gene and associations with plasma FVIII activity levels.Segregation distortion of the CTG repeats at the myotonic dystrophy locus.Design and analysis of effects of triplet repeat oligonucleotides in cell models for myotonic dystrophy Triplet-repeat oligonucleotide-mediated reversal of RNA toxicity in myotonic dystrophy.Polymorphisms of the glucocorticoid receptor gene in laboratory and wild rats: steroid binding properties of trinucleotide CAG repeat length variants.FMR1 in global populations CTG repeat polymorphism in DMPK gene in healthy Yugoslav population.Transmission ratio distortion in the myotonic dystrophy locus in human preimplantation embryos.Distribution of CTG repeats at the DMPK gene in myotonic dystrophy patients and healthy individuals from the Mexican population.

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P2860

Normal variation at the myotonic dystrophy locus in global human populations.

http://www.wikidata.org/entity/Q41972483

description

1995 nî lūn-bûn

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1995年の論文

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1995年論文

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1995年論文

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1995年論文

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1995年論文

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1995年論文

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1995年论文

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1995年论文

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1995年论文

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name

Normal variation at the myotonic dystrophy locus in global human populations.

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type

label

Normal variation at the myotonic dystrophy locus in global human populations.

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prefLabel

Normal variation at the myotonic dystrophy locus in global human populations.

@en

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American Journal of Human Genetics

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Normal variation at the myotonic dystrophy locus in global human populations.

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A Torroni

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C Zerylnick

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S L Sherman

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S T Warren

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P2860

Southeast Asian mitochondrial DNA analysis reveals genetic continuity of ancient mongoloid migrations.

Native American mitochondrial DNA analysis indicates that the Amerind and the Nadene populations were founded by two independent migrations.

Asian affinities and continental radiation of the four founding Native American mtDNAs

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations

French myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertion

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.

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123-130

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