<scp> <i>SCN10A</i> </scp> variants associated with congenital harlequin syndrome-Reference-Cited by-同舟云学术

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SCN10A variants associated with congenital harlequin syndrome

Published:2022-03-22 Issue:6 Volume:186 Page:1039-1041
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br J Dermatol

Author:

Halle Aurelie¹^ORCID,De Becdelievre Alix²,Funalot Benoit²,Labrèze Christine³,Morice‐Picard Fanny³^ORCID,Boralevi Franck³

Affiliation:

1. Department of Dermatology Centre Hospitalier Universitaire d’Amiens Amiens France

2. Department of Medical Genetics Henri Mondor University Hospital, AP‐HP, INSERM, IMRB, Paris Est Créteil University Créteil France

3. Department of Dermatology and Pediatric Dermatology, National Reference Centre for Rare Disorders Hôpital des Enfants Pellegrin, Centre Hospitalier Universitaire de Bordeaux Bordeaux France

Publisher

Oxford University Press (OUP)

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjd.21011

Reference7 articles.

1. Harlequin syndrome: the sudden onset of unilateral flushing and sweating.

2. Congenital Harlequin syndrome as an isolated phenomenon: A case report and review of the literature

3. Child Neurology: An infant with episodic facial flushing

4. Paroxysmal extreme pain disorder in family with c.3892G > T (p.Val1298Phe) in the SCN9A gene mutation – case report;Stępień A;BMC Neurol,2020

5. Painful and painless channelopathies

Cited by 1 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. Idiopathic Harlequin syndrome.;Russian neurological journal;2023-11-26

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