A novel large deletion of the CYLD gene causes CYLD cutaneous syndrome in a Chinese family-Reference-Cited by-同舟云学术

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A novel large deletion of the CYLD gene causes CYLD cutaneous syndrome in a Chinese family

Published:2020-08-11 Issue:10 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Zhu Ruizheng¹^ORCID,Xu Jie²,Shen Juan¹,Li Wenru²,Tan Fei¹,Li Changchang²,Wei Zhichen²,Liu Yeqiang¹,Bai Yun¹^ORCID

Affiliation:

1. Shanghai Skin Disease Hospital Tongji University School of Medicine Shanghai China

2. Wenzhou Hospital of Integrated Traditional Chinese and Western Medicine Wenzhou City China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1441

Reference18 articles.

1. Identification of the familial cylindromatosis tumour-suppressor gene

2. Mutations in the CYLD gene in Brooke–Spiegler Syndrome, Familial Cylindromatosis, and Multiple Familial Trichoepithelioma: Lack of Genotype–Phenotype Correlation

3. Loss of the cylindromatosis tumour suppressor inhibits apoptosis by activating NF-κB

4. Epigenetic modifiers DNMT3A and BCOR are recurrently mutated in CYLD cutaneous syndrome

5. Occurrence of basal cell carcinoma among multiple trichoepitheliomas

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Repressive Control of Keratinocyte Cytoplasmic Inflammatory Signaling;International Journal of Molecular Sciences;2023-07-26

2. Tumores cutáneos múltiples en el polo cefálico. Diagnóstico y comentario;Piel;2022-04

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