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J Eur Acad Dermatol Venereol. 2017 May;31(5):e230-e232. doi: 10.1111/jdv.14042. Epub 2016 Dec 2.

Exome sequencing identifies FATP1 mutation in Melkersson-Rosenthal syndrome.

Xu XG1,2, Guan LP3, Lv Y4, Wan YS5, Wu Y1,2, Qi RQ1,2, Liu ZG6, Zhang JG3, Chen YL3, Xu FP3, Xu X3, Li YH1,2, Geng L1,2, Gao XH1,2, Chen HD1,2.

Author information

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.
PMID:
27862329
DOI:
10.1111/jdv.14042
[Indexed for MEDLINE]

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