Autosomal Dominant Erythermalgia Associated With a Novel Mutation in the Voltage-Gated Sodium Channel α Subunit Nav1.7-Reference-Cited by-同舟云学术

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Autosomal Dominant Erythermalgia Associated With a Novel Mutation in the Voltage-Gated Sodium Channel α Subunit Nav1.7

Published:2005-10-01 Issue:10 Volume:62 Page:
ISSN:0003-9942
Container-title:Archives of Neurology
language:en
Short-container-title:Arch Neurol

Author:

Michiels Jan J.,te Morsche Rene H. M.,Jansen Jan B. M. J.,Drenth Joost P. H.

Publisher

American Medical Association (AMA)

Subject

Clinical Neurology,Arts and Humanities (miscellaneous)

Cited by 81 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Dermatoses Resulting from Disorders of the Veins and Arteries;Rook's Textbook of Dermatology;2024-02-20

2. Erythromelalgia caused by the missense mutation p.Arg220Pro in an alternatively spliced exon of SCN9A (NaV1.7);Human Molecular Genetics;2023-09-18

3. Voltage Gated Sodium Channel Genes in Epilepsy: Mutations, Functional Studies, and Treatment Dimensions;Frontiers in Neurology;2021-03-24

4. No association between SCN9A and monogenic human epilepsy disorders;PLOS Genetics;2020-11-20

5. Computational pipeline to probe NaV1.7 gain-of-function variants in neuropathic painful syndromes;Scientific Reports;2020-10-21

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