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

Crossref DOI link: https://doi.org/10.15252/emmm.202114904

Published Online: 2022-04

Published Print: 2022-05-09

Update policy: https://doi.org/10.1002/crossmark_policy

Authors

Chen, Fuying https://orcid.org/0000-0002-7439-4845
Ni, Cheng

Wang, Xiaoxiao https://orcid.org/0000-0003-3490-6735
Cheng, Ruhong

Pan, Chaolan https://orcid.org/0000-0003-3378-4676
Wang, Yumeng

Liang, Jianying

Zhang, Jia

Cheng, Jinke https://orcid.org/0000-0002-4344-5363
Chin, Y Eugene https://orcid.org/0000-0003-4962-1396
Zhou, Yi https://orcid.org/0000-0002-7785-7112
Wang, Zhen

Guo, Yiran

Chen, She

Htun, Stephanie

Mathes, Erin F

de Alba Campomanes, Alejandra G

Slavotinek, Anne M

Zhang, Si https://orcid.org/0000-0002-5682-4995
Li, Ming https://orcid.org/0000-0003-3053-2756
Yao, Zhirong https://orcid.org/0000-0003-0785-8985
Funding

Funding for this research was provided by:

National Natural Science Foundation of China (81874239)

National Natural Science Foundation of China (82073422)

National Natural Science Foundation of China (81630083)

National Natural Science Foundation of China (81874252)
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Publication History

Received: 2021-09-02

Accepted: 2022-03-08

Published: 2022-04-01