Novel mutations in one allele in a Chinese family with neurofibromatosis type 1: Including a complex insertion–deletion mutation-Reference-Cited by-同舟云学术

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Novel mutations in one allele in a Chinese family with neurofibromatosis type 1: Including a complex insertion–deletion mutation

Published:2016-07-04 Issue:11 Volume:43 Page:1332-1335
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Zhu Lude¹,Shi Lei¹,Wang Bo²,Bi Mingye³,Pu Jie³,Zhang Linglin¹,Zhang Yunfeng¹,Wang Xiuli¹,Zhang Guolong¹

Affiliation:

1. Institute of Photomedicine Shanghai Skin Disease Hospital Tongji University School of MedicineShanghai China

2. Department of Dermatology Ruijin Hospital Shanghai Jiaotong University School of Medicine Shanghai China

3. Department of Dermatology Nanjing Medical University Affiliated Wuxi People's Hospital Wuxi China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.13498

Reference13 articles.

1. Neurofibromatosis Type 1 Revisited

2. Neurofibromatosis

3. Forensic Considerations in Cases of Neurofibromatosis?An Overview

4. The Genetic and Molecular Pathogenesis of NF1 and NF2

5. Expression ofNF1pseudogenes

Cited by 3 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. Exuberant manifestation of neurofibromatosis type 1 affecting 3 generations: delayed diagnosis and the importance of the multidisciplinary approach;Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology;2019-09

2. Surgical Treatment of a Massive Neurofibroma of the Head and Neck in a Patient with Neurofibromatosis Type 1: A Case Report;International Journal of Morphology;2018-03

3. Homozygous frame-shift mutation in a Chinese family with neurofibromatosis type 1;The Journal of Dermatology;2017-11-30

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