Exome sequencing identifies FATP1 mutation in Melkersson-Rosenthal syndrome-Reference-Cited by-同舟云学术

Exome sequencing identifies FATP1 mutation in Melkersson-Rosenthal syndrome

Published:2016-12-02 Issue:5 Volume:31 Page:e230-e232
ISSN:0926-9959
Container-title:Journal of the European Academy of Dermatology and Venereology
language:en
Short-container-title:J Eur Acad Dermatol Venereol

Author:

Xu X.G.¹²,Guan L.P.³,Lv Y.⁴,Wan Y.S.⁵,Wu Y.¹²,Qi R.Q.¹²,Liu Zh.G.⁶,Zhang J.G.³,Chen Y.L.³,Xu F.P.³,Xu X.³,Li Y.H.¹²,Geng L.¹²,Gao X.H.¹²,Chen H.D.¹²

Affiliation:

1. Department of Dermatology; No.1 Hospital of China Medical University; Shenyang 110001 China

2. Key Laboratory of Immunodermatology; National Health and Family Planning Commission of the People's Republic of China; Shenyang 110001 China

3. BGI-Shenzhen; Shenzhen Guangdong Province 518083 China

4. Liaoning Centre for Prenatal Diagnosis; Department of Gynecology & Obstetrics; Shengjing Hospital of China Medical University; Shenyang 110004 China

5. Department of Biology; Providence College; Providence RI 02918 USA

6. Molecular Pharmacology Research Center; School of Pharmaceutical Sciences; Wenzhou Medical University; Wenzhou 325035 China

Publisher

Wiley

Subject

Infectious Diseases,Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jdv.14042/fullpdf

Reference10 articles.

1. Melkersson-Rosenthal syndrome: a facial nerve center perspective;Rivera-Serrano;J Plast Reconstr Aesthet Surg,2014

2. Melkersson-Rosenthal syndrome with genitalia involved in a 12-year-old boy;Chu;Ann Dermatol,2016

3. Family study on Melkersson-Rosenthal syndrome. Some hereditary aspects of the disease and review of literature;Meisel-Stosiek;Acta Derm Venereol,1990

4. TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing;Wang;Brain,2010

5. Exome sequencing identifies ZNF644 mutations in high myopia;Shi;PLoS Genet,2011

Cited by 18 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. Skin and Lacrimal Drainage System;Ocular Pathology;2025

2. Melkersson–Rosenthal syndrome: A case report;Clinical Case Reports;2024-02

3. Melkersson–Rosenthal Syndrome and Migraine: A New Phenotype Associated with SCN1A Variants?;Genes;2023-07-20

4. Myeloid-specific fatty acid transport protein 4 deficiency induces a sex-dimorphic susceptibility for nonalcoholic steatohepatitis in mice fed a high-fat, high-cholesterol diet;American Journal of Physiology-Gastrointestinal and Liver Physiology;2023-05-01

5. Melkersson–Rosenthal syndrome. Clinical case;Russian Journal of Skin and Venereal Diseases;2022-05-12