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Multiple squamous cell carcinomas arising on an epidermal nevus harboring HRAS p.G13R mutation.

作者信息

Narahira Atsushi, Kitamura Shinya, Maeda Takuya, Nishihara Hiroshi, Yanagi Teruki

机构信息

Department of Dermatology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

Genomics Unit, Keio Cancer Center, Keio University School of Medicine, Tokyo, Japan.

出版信息

J Dermatol. 2021 Feb;48(2):e92-e93. doi: 10.1111/1346-8138.15682. Epub 2020 Nov 8.

DOI:10.1111/1346-8138.15682
PMID:33161608
Abstract
摘要

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引用本文的文献

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A Child with Cutaneous-Skeletal Hypophosphatemia Syndrome Caused by a Mosaic HRAS Mutation: Outcome of Treatment with Anti-FGF23 Antibody.一名因HRAS基因镶嵌突变导致皮肤骨骼低磷血症综合征的儿童:抗FGF23抗体治疗的结果
Calcif Tissue Int. 2025 Apr 28;116(1):65. doi: 10.1007/s00223-025-01373-x.
2
Case Report: Sequential postzygotic mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving in oncogenic transformation.病例报告:一名患有表皮痣和横纹肌肉瘤的患者中,携带突变等位基因的父源11号染色体发生了合子后序列突变和增益:涉及致癌转化的多重打击机制的证据。
Front Genet. 2023 Aug 10;14:1231434. doi: 10.3389/fgene.2023.1231434. eCollection 2023.