S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis‐like syndrome

Author:

Chen Fuying12ORCID,Ni Cheng12,Wang Xiaoxiao12ORCID,Cheng Ruhong12,Pan Chaolan12ORCID,Wang Yumeng12,Liang Jianying1,Zhang Jia1,Cheng Jinke3ORCID,Chin Y Eugene4ORCID,Zhou Yi5ORCID,Wang Zhen6,Guo Yiran7,Chen She8,Htun Stephanie9,Mathes Erin F10,de Alba Campomanes Alejandra G11,Slavotinek Anne M9,Zhang Si8ORCID,Li Ming12ORCID,Yao Zhirong12ORCID

Affiliation:

1. Department of Dermatology Xinhua Hospital Shanghai Jiaotong University School of Medicine Shanghai China

2. Institute of Dermatology Shanghai Jiaotong University School of Medicine Shanghai China

3. Shanghai Key Laboratory for Tumor Microenvironment and Inflammation Department of Biochemistry and Molecular Cell Biology Shanghai Jiao Tong University School of Medicine Shanghai China

4. Instituteof Health Sciences, Chinese Academy of Sciences Shanghai Jiaotong University School of Medicine Shanghai China

5. Department of gastroenterology Zhongshan Hospital Fudan University Shanghai China

6. Department of Dermatology Children's Hospital of Shanghai Jiaotong University Shanghai China

7. Center for Data Driven Discovery in Biomedicine Children’s Hospital of Philadelphia PA USA

8. NHC Key Laboratory of Glycoconjugate Research Department of Biochemistry and Molecular Biology School of Basic Medical Sciences Fudan University Shanghai China

9. Division of Genetics Department of Pediatrics University of California San Francisco San Francisco CA USA

10. Departments of Dermatology and Pediatrics University California San Francisco CA USA

11. Department of Ophthalmology University of California San Francisco CA USA

Funder

National Natural Science Foundation of China

Publisher

EMBO

Subject

Molecular Medicine

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