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

Molecular and clinical study of two myotonic dystrophy homozygotes.

Journal of medical genetics - 1 Nov 2001

Akbas F, Serdaroglu P, Deymeer F, Aysal F, Erginel-Unaltuna N

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to DNA
Share to Homozygote
Share to Myotonic Dystrophy

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Myotonin-Protein Kinase

Share to Protein Serine-Threonine Kinases

Share to Trinucleotide Repeat Expansion

Share to Trinucleotide Repeats

Source

Open in PubMed Open full text

Identifiers

PMID: 11694554
DOI: 10.1136/jmg.38.11.e40
PMCID: PMC1734760

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

Molecular and clinical study of two myotonic dystrophy homozygotes.PMID 11694554Read ↗

[Clinical and molecular genetical features of myotonic dystrophy].Semantic proximity Read ↗

Myotonic dystrophySemantic proximity Read ↗

Mutations, molecules, and myotonia.Semantic proximity Read ↗

Genetic mapping of a second myotonic dystrophy locusSemantic proximity Read ↗

Changing clinical concepts of Duchenne muscular dystrophy: molecular genetic diagnosis.Semantic proximity Read ↗

Genetics and the muscular dystrophies.Semantic proximity Read ↗

Molecular genetics of Duchenne muscular dystrophy.Semantic proximity Read ↗

The Emery-Dreifuss Muscular Dystrophy Mutation Database.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: DMD. Disease: muscular dystrophy, Duchenne.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: DMD. Disease: muscular dystrophy, Duchenne.Semantic proximity Read ↗

[Recommendations of good practices for the genetic diagnosis of myotonic dystrophy. Grupo AEGH/CIBERER].Semantic proximity Read ↗

Muscular Dystrophies and Other Genetic MyopathiesSemantic proximity Read ↗

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