Natural history of TRPV4-Related disorders: From skeletal dysplasia to neuromuscular phenotype
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Reference41 articles.
1. TRPV4 channel participates in receptor-operated calcium entry and ciliary beat frequency regulation in mouse airway epithelial cells;Lorenzo;Proc. Natl. Acad. Sci. U. S. A.,2008
2. TRPV4-mediated channelopathies;Verma;Channels,2010
3. Nosology and classification of genetic skeletal disorders: 2019 revision;Mortier;Am. J. Med. Genet.,2019
4. Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia;Rock;Nat. Genet.,2008
5. Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4;Deng;Nat. Genet.,2010
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1. Case Report: TRPV4 gene mutation causing neuronopathy, distal hereditary motor, type VIII;Frontiers in Pediatrics;2024-03-18
2. Genetically Regulated Gene Expression in the Brain Associated With Chronic Pain: Relationships With Clinical Traits and Potential for Drug Repurposing;Biological Psychiatry;2023-09
3. Astrocytic TRPV4 Channels and Their Role in Brain Ischemia;International Journal of Molecular Sciences;2023-04-12
4. Chronic pain gene expression changes in the brain and relationships with clinical traits;2022-12-30
5. Radiographical Survey of Osteochondrodysplasia in Scottish Fold Cats caused by the TRPV4 gene variant;Human Genetics;2021-08-18
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