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

A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3

1 Sept 1999

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 Hereditary Neurological Disorders
Share to Neurological diseases and metabolism
Share to Peripheral Neuropathies and Disorders

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 10441578
DOI: 10.1086/302542

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3PMID 10441578Read ↗

Axonal Charcot–Marie–Tooth diseaseSemantic 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 ↗

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

Axonal Charcot-Marie-Tooth Disease: from Common Pathogenic Mechanisms to Emerging Treatment Opportunities.Semantic proximity Read ↗

A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease.Semantic proximity Read ↗

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

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

A second locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 19q13.3.Semantic proximity Read ↗

Mapping of Charcot-Marie-Tooth Disease Type 1C to Chromosome 16p Identifies a Novel Locus for Demyelinating NeuropathiesSemantic proximity Read ↗

Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inherited disease.Semantic proximity Read ↗

Charcot-Marie-Tooth disease: an updateSemantic proximity Read ↗

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