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

Incidence and Clinical Features of TRPV4-Linked Axonal Neuropathies in a USA Cohort of Charcot–Marie–Tooth Disease Type 2

29 Aug 2019

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 Whipple's Disease and Interleukins

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 31468327
DOI: 10.1007/s12017-019-08564-4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Incidence and Clinical Features of TRPV4-Linked Axonal Neuropathies in a USA Cohort of Charcot–Marie–Tooth Disease Type 2PMID 31468327Read ↗

Striking phenotypic variability in familial TRPV4-axonal neuropathy spectrum disorder.Semantic proximity Read ↗

Phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathy.Semantic proximity Read ↗

TRPV4 axonal neuropathy spectrum disorder.Semantic proximity Read ↗

Phenotypic variability of TRPV4 related neuropathies.Semantic proximity Read ↗

Update on Charcot-Marie-Tooth disease.Semantic proximity Read ↗

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

Charcot-Marie-Tooth Disease and Other Hereditary NeuropathiesSemantic proximity Read ↗

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

Charcot-Marie-Tooth neuropathies: diagnosis and management.Semantic proximity Read ↗

[Hereditary motor-sensory neuropathies (Charcot-Marie-Tooth syndrome) and related neuropathies. Current classification and genotype-phenotype correlation].Semantic proximity Read ↗

Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4.Semantic proximity Read ↗

Peripheral Neuropathy: A Phenotype-Driven Review for Diagnosis and Management.Semantic proximity Read ↗

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