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

Genetic basis of inherited peripheral neuropathies.

Human mutation - 1 Jan 1994

Suter U, Patel P I

Abstract excerpt

Progress in the elucidation of the genetic basis for inherited peripheral neuropathies has been remarkable over the last years. In particular, the molecular mechanisms underlying the autosomal dominantly inherited disorders Charcot-Marie-Tooth disease type 1A (CMT1A), Charcot-Marie-Tooth disease type 1B (CMT1B), and hereditary neuropathy with liability to pressure palsies (HNPP) have been determined. While...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 17
Share to Genes
Share to Genotype

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

Share to Multigene Family

Share to Phenotype

Share to Point Mutation

Share to Sequence Deletion

Source

Identifiers

PMID: 7515304
DOI: 10.1002/humu.1380030203

Genes

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

Genetic basis of inherited peripheral neuropathies.PMID 7515304Read ↗

Clinical features and molecular genetics of hereditary peripheral neuropathies.Semantic proximity Read ↗

Genetic mechanisms of peripheral nerve disease.Semantic proximity Read ↗

Inherited neuropathies: Charcot-Marie-Tooth disease and related disorders.Semantic proximity Read ↗

Dominantly inherited peripheral neuropathies.Semantic proximity Read ↗

Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies.Semantic proximity Read ↗

[Advances in the molecular genetics of the hereditary neuropathies].Semantic proximity Read ↗

Molecular genetics of inherited peripheral neuropathies: who are the actors?Semantic proximity Read ↗

Molecular mechanisms, diagnosis, and rational approaches to management of and therapy for Charcot-Marie-Tooth disease and related peripheral neuropathies.Semantic proximity Read ↗

Charcot-Marie-Tooth disease type 1A: mutational mechanisms and candidate gene.Semantic proximity Read ↗

Deletion of the PMP22 gene and hereditary neuropathy with liability to pressure palsies.Semantic proximity Read ↗

Molecular genetics of peripheral neuropathies.Semantic proximity Read ↗

Inherited primary peripheral neuropathies. Molecular genetics and clinical implications of CMT1A and HNPP.Semantic proximity Read ↗

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