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 genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease.

Neuromolecular medicine - 1 Jan 2006

Houlden Henry, Reilly Mary M

Abstract excerpt

Charcot-Marie-Tooth disease (CMT) is a clinically and genetically heterogeneous group of disorders and is the most common inherited neuromuscular disorder, with an estimated overall prevalence of 17-40/10,000. Although there has been major advances in the understanding of the genetic basis of CMT in recent years, the most useful classification is still a neurophysiological classification that divides CMT into...

Read the complete abstract on PubMed

Topics

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

Share to Charcot-Marie-Tooth Disease
Share to Chromosome Disorders
Share to Demyelinating Diseases

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

Share to Early Growth Response Protein 2

Share to Myelin P0 Protein

Share to Myelin Proteins

Share to Nerve Fibers, Myelinated

Share to Neurofilament Proteins

Source

Identifiers

PMID: 16775366
DOI: 10.1385/nmm:8:1-2:43

Genes

EGR2
LITAF
MPZ
NEFL
PMP22

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease.PMID 16775366Read ↗

Molecular genetics of autosomal-recessive axonal Charcot-Marie-Tooth neuropathies.Semantic proximity Read ↗

[Charcot-Marie-Tooth disease].Semantic proximity Read ↗

[Autosomal recessive forms of Charcot-Marie-Tooth disease].Semantic proximity Read ↗

Autosomal recessive Charcot-Marie-Tooth disease: from genes to phenotypes.Semantic proximity Read ↗

Autosomal recessive Charcot-Marie-Tooth neuropathy.Semantic proximity Read ↗

Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease.Semantic proximity Read ↗

Molecular genetics of autosomal-dominant axonal Charcot-Marie-Tooth disease.Semantic proximity Read ↗

Charcot‐Marie‐Tooth Disease: A Clinico‐genetic ConfrontationSemantic proximity Read ↗

Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in JapanSemantic proximity Read ↗

Charcot-Marie-Tooth disease and related genetic neuropathies.Semantic proximity Read ↗

Autosomal recessive forms of Charcot-Marie-Tooth disease.Semantic proximity Read ↗

Molecular characterization of Turkish patients with demyelinating Charcot-Marie-Tooth disease.Semantic proximity Read ↗

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