Corrigendum: Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene

Min Zhou; Ningjie Shi; Juan Zheng; Yang Chen; Siqi Wang; Kangli Xiao; Zhenhai Cui; Kangli Qiu; Feng Zhu; Huiqing Li

doi:10.3389/fendo.2022.856002

Corrigendum: Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene

Front Endocrinol (Lausanne). 2022 Feb 21:13:856002. doi: 10.3389/fendo.2022.856002. eCollection 2022.

Authors

Min Zhou^{1

2}, Ningjie Shi^{3

4}, Juan Zheng^{3

4}, Yang Chen^{3

4}, Siqi Wang^{3

4}, Kangli Xiao^{3

4}, Zhenhai Cui^{3

4}, Kangli Qiu^{3

4}, Feng Zhu^{5

6}, Huiqing Li^{3

4}

Affiliations

¹ Department of Pulmonary and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
² Key Laboratory of Respiratory Diseases, National Ministry of Health of the People's Republic of China and National Clinical Research Center for Respiratory Disease, Wuhan, China.
³ Department of Endocrinology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
⁴ Hubei Provincial Clinical Research Center for Diabetes and Metabolic Disorders, Wuhan, China.
⁵ Clinic Center of Human Gene Research, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
⁶ Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Abstract

[This corrects the article DOI: 10.3389/fendo.2021.770871.].

Keywords: Woodhouse–Sakati syndrome; alopecia; diabetes; hypogonadism; intellectual disability.

Publication types

Published Erratum