Corrigendum: Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene
- PMID: 35265045
- PMCID: PMC8900264
- 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
Abstract
[This corrects the article DOI: 10.3389/fendo.2021.770871.].
Keywords: Woodhouse–Sakati syndrome; alopecia; diabetes; hypogonadism; intellectual disability.
Copyright © 2022 Zhou, Shi, Zheng, Chen, Wang, Xiao, Cui, Qiu, Zhu and Li.
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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). 2021 Dec 23;12:770871. doi: 10.3389/fendo.2021.770871. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 35002959 Free PMC article.
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