Erythromelalgia: A Child With V400M Mutation in the SCN9A Gene-Reference-Cited by-同舟云学术

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Erythromelalgia: A Child With V400M Mutation in the SCN9A Gene

Published:2021-03-01 Issue:2 Volume:7 Page:e570
ISSN:2376-7839
Container-title:Neurology Genetics
language:en
Short-container-title:Neurol Genet

Author:

Nwebube Chineze,Bulancea Sabrina,Marchidann Adrian,Bello-Espinosa Lourdes,Treidler Simona

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),Neurology (clinical)

Reference7 articles.

1. Severe case and literature review of primary erythromelalgia: Novel SCN9A gene mutation

2. PINK1 autophosphorylation upon membrane potential dissipation is essential for Parkin recruitment to damaged mitochondria

3. A novel Nav1.7 mutation producing carbamazepine-responsive erythromelalgia

4. Erythermalgia: molecular basis for an inherited pain syndrome

5. A case of inherited erythromelalgia

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1. Exploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathy;Journal of Neurogenetics;2024-04-02

2. Erythromelalgia: A Review of Medical Management Options and Our Approach to Management;Mayo Clinic Proceedings;2023-01

3. Amitriptyline/gabapentin;Reactions Weekly;2021-10

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