Homozygous frame-shift mutation in a Chinese family with neurofibromatosis type 1-Reference-Cited by-同舟云学术

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Homozygous frame-shift mutation in a Chinese family with neurofibromatosis type 1

Published:2017-11-30 Issue:5 Volume:45 Page:e134-e135
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Yang Jian-Kang¹^ORCID,Wu Wen-Juan²,He Li²

Affiliation:

1. Department of Biochemistry and Molecular Biology; Dali University; Dali China

2. Department of Dermatology; First Affiliated Hospital of Kunming Medical University; Kunming China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Yunnan Province

Science Foundation for The Doctor of Dali University

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/1346-8138.14165/fullpdf

Reference5 articles.

1. Molecular characterization of NF1 and neurofibromatosis type 1 genotype-phenotype correlations in a Chinese population;Zhang;Sci Rep,2015

2. Clinical and molecular characterization of NF1 patients: single-center experience of 32 patients from China;Zhu;Medicine,2016

3. The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis2;Gutmann;JAMA,1997

4. Novel mutations in one allele in a Chinese family with neurofibromatosis type 1: including a complex insertion-deletion mutation;Zhu;J Dermatol,2016

5. Clinical, pathologic, and genetic features of massive soft tissue neurofibromas in a Sicilian patient;Bongiorno;Dermatol Ther,2008

Cited by 1 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. NF1, Neurofibromin and Gene Therapy: Prospects of Next-Generation Therapy;Current Gene Therapy;2020-09-18

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