Gain‐of‐function mutation Met136Val in SCN8A may not be a common cause of trigeminal neuralgia
Author:
Affiliation:
1. Department of Neurosurgery School of Medicine University of Pittsburgh Pittsburgh PA USA
2. Department of Oral Biology School of Dental Medicine University of Pittsburgh Pittsburgh PA USA
Publisher
Wiley
Subject
Genetics(clinical),Genetics,Molecular Biology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1587
Reference6 articles.
1. No Association of Polymorphisms in Nav1.7 or Nerve Growth Factor Receptor Genes with Trigeminal Neuralgia
2. Cranial neuralgias;Cruccu G.;The Handbook of Clinical Neurology,2010
3. Comparative study of five commercially available saliva collection kits for DNA extraction;Deeley K.;Clinical Laboratory,2016
4. Familial trigeminal neuralgia – a systematic clinical study with a genomic screen of the neuronal electrogenisome
5. Hammer M. F. Wagnon J. L. Mefford H. C. Meisler M. H. Adam M. P. Ardinger H. H. Pagon R. A. Wallace S. E. Bean L. J. H. Stephens K. &Amemiya A.(2016).SCN8A‐related epilepsy with encephalopathy. GeneReviews® [Internet]. :University of Washington. 1993–2020.
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1. Trigeminal neuralgia;Nature Reviews Disease Primers;2024-05-30
2. The pathophysiology of trigeminal neuralgia: a molecular review;Journal of Neurosurgery;2023-03-01
3. Classical trigeminal neuralgia is associated with gephyrin and sodium voltage-gated channel alpha subunit 8;Frontiers in Dental Medicine;2023-01-30
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