A new frameshift mutation in a patient with neurofibromatosis type I
Eur J Dermatol
.
2023 Dec 1;33(6):697-699.
doi: 10.1684/ejd.2023.4580.
Authors
Zhongzhu Hu
1
,
Mengling Zhou
2
,
Zilu Zeng
3
,
He Huang
1
,
Meng Zhang
1
,
Jiahua Zou
1
,
Guang-Ming Xia
1
,
Yan Wu
2
,
Jiabin Yang
4
,
Nengxing Lin
2
Affiliations
1
Huanggang Central Hospital of Yangtze University, Huanggang, China.
2
Department of Dermatology, Union Hospital Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
3
Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
4
Department of Dermatology, the first Affiliated Hospital of Yangtze University, Jingzhou, China.
PMID:
38465558
DOI:
10.1684/ejd.2023.4580
No abstract available
MeSH terms
Frameshift Mutation
Genes, Neurofibromatosis 1
Humans
Mutation
Neurofibromatosis 1* / complications
Neurofibromatosis 1* / genetics
Neurofibromin 1 / genetics
Pedigree
Substances
Neurofibromin 1