Two novel SCN9A mutations causing insensitivity to pain-Reference-Cited by-同舟云学术

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Two novel SCN9A mutations causing insensitivity to pain

Published:2009-05 Issue:1 Volume:143 Page:155-158
ISSN:0304-3959
Container-title:Pain
language:en
Short-container-title:

Author:

Nilsen K. B.,Nicholas A. K.,Woods C. G.,Mellgren S. I.,Nebuchennykh M.,Aasly J.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Anesthesiology and Pain Medicine,Clinical Neurology,Neurology

Reference14 articles.

1. A stop codon mutation in SCN9A causes lack of pain sensation.;Ahmad;Hum Mol Genet,2007

2. Molecular genetics of hereditary sensory neuropathies.;Auer-Grumbach;Neuromolecular Med,2006

3. An SCN9A channelopathy causes congenital inability to experience pain.;Cox;Nature,2006

4. From genes to pain: Nav1.7 and human pain disorders.;Dib-Hajj;Trends Neurosci,2007

5. Development of the 12-Item Cross-Cultural Smell Identification Test(CC-SIT).;Doty;Laryngoscope,1996

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1. Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain;International Journal of Molecular Sciences;2024-06-08

2. Identification and In-Silico study of non-synonymous functional SNPs in the human SCN9A gene;PLOS ONE;2024-02-23

3. Human pain channelopathies;Handbook of Clinical Neurology;2024

4. Structural basis for NaV1.7 inhibition by pore blockers;Nature Structural & Molecular Biology;2022-11-24

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