A heterozygous mutation in the RAG2 gene with cutaneous and systemic manifestations partially resembling Omenn syndrome-Reference-Cited by-同舟云学术

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A heterozygous mutation in the RAG2 gene with cutaneous and systemic manifestations partially resembling Omenn syndrome

Published:2021-06 Issue:6 Volume:19 Page:906-908
ISSN:1610-0379
Container-title:JDDG: Journal der Deutschen Dermatologischen Gesellschaft
language:de
Short-container-title:JDDG: Journal der Deutschen Dermatologischen Gesellschaft

Author:

Estébanez Andrea¹,Verdú‐Amorós Jaime²,Silva Esmeralda¹,Velasco Rebeca¹,Cuesta Ana³,Monteagudo Carlos⁴,Martín Jose M.¹

Affiliation:

1. Department of Dermatology Clinical University Hospital University of Valencia Valencia Spain

2. Department of Paediatric Clinical University Hospital University of Valencia Valencia Spain

3. Department of Genetics Clinical University Hospital University of Valencia Valencia Spain

4. Department of Pathology Clinical University Hospital University of Valencia Valencia Spain

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ddg.14383

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. From variant of uncertain significance to likely pathogenic in two siblings with atypical RAG2 Deficiency: a case report and review of the literature;BMC Pediatrics;2024-02-13

2. Hematopoietic Stem Cell Transplantation for Omenn Syndrome: A Case Report;Advances in Clinical Medicine;2023

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