Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Correlation between the incidence of myotonic dystrophy in different groups in Israel and the number of CTG trinucleotide repeats in the myotonin gene.

American journal of medical genetics - 8 Aug 1997

Mor-Cohen R, Magal N, Gadoth N, Shohat T, Shohat M

Abstract excerpt

Myotonic dystrophy (DM) is associated with an increased number of CTG repeats in the 3' untranslated region of the myotonin gene. Because DM has been observed less frequently in Ashkenazic Jews and non-Jews than in North African and Yemenite Jews in Israel, a study of the CTG repeat polymorphism was undertaken in these four groups. Alleles from 126 unrelated healthy North African Jews, 103 Yemenite Jews, 103...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to Blotting, Southern

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to DNA Primers

Share to Polymerase Chain Reaction

Share to Polymorphism, Genetic

Share to Pregnancy

Share to Proteins

Source

Identifiers

PMID: 9217214
DOI: 10.1002/(sici)1096-8628(19970808)71:2<156::aid-ajmg7>3.0.co;2-w

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Correlation between the incidence of myotonic dystrophy in different groups in Israel and the number of CTG trinucleotide repeats in the myotonin gene.PMID 9217214Read ↗

Prevalence of myotonic dystrophy in Israeli Jewish communities: inter-community variation and founder premutations.Semantic proximity Read ↗

Absence of myotonic dystrophy in southern African Negroids is associated with a significantly lower number of CTG trinucleotide repeats.Semantic proximity Read ↗

Distribution of CTG repeats at the DMPK gene in myotonic dystrophy patients and healthy individuals from the Mexican population.Semantic proximity Read ↗

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.Semantic proximity Read ↗

Correlations between individual clinical manifestations and CTG repeat amplification in myotonic dystrophy.Semantic proximity Read ↗

Normal variation at the myotonic dystrophy locus in global human populations.Semantic proximity Read ↗

Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in Israel.Semantic proximity Read ↗

[Normal polymorphism of the (CTG)n repeat in the myotonin protein kinase (DM) gene on chromosome 19q13.3 in Western European populations].Semantic proximity Read ↗

Genotype-phenotype correlation in myotonic dystrophy.Semantic proximity Read ↗

[Population analysis CTG trinucleotide repeats in the myotonin-protein kinase I gene].Semantic proximity Read ↗

Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations.Semantic proximity Read ↗

Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeatsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.