Clear Search sequence regions


Sizes of these terms reflect their relevance to your search.

To explore the genetic basis for a Chinese pedigree and a sporadic case with Neurofibromatosis type 1 (NF1). Clinical data of the pedigree and the sporadic case were collected. Genomic DNA was extracted from peripheral venous blood samples and subjected to whole exome sequencing. Candidate variants were validated by Sanger sequencing and bioinformatic analysis. All patients from the pedigree were found to harbor a c.3251delC variant in exon 25 of the NF1 gene, whilst a c.4312_4314delGAA variant was found in exon 32 of the NF1 gene in the sporadic case. Variants of the NF1 gene may account for the occurrence of NF1 in this pedigree and sporadic case.

Citation

Xiaoyan Zhao, Kunli Zhou, Qiguo Zhang, Liangqi Cai. Analysis of NF1 gene variants in a Chinese pedigree and a sporadic patient with Neurofibromatosis type 1]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 2024 Mar 10;41(3):317-321

Expand section icon Mesh Tags

Expand section icon Substances


PMID: 38448021

View Full Text