Identification of two novel nonsense mutations in the transglutaminase 1 gene in a Hungarian patient with congenital ichthyosiform erythroderma
Author:
Publisher
Wiley
Subject
Dermatology,Molecular Biology,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1600-0625.2003.120313.x/fullpdf
Reference22 articles.
1. The complexity and redundancy of epithelial barrier function;Steinert;J Cell Biol,2000
2. Linkage of autosomal recessive lamellar ichthyosis to chromosome 14q;Russell;Am J Hum Genet,1994
3. Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated population;Laiho;Am J Hum Genet,1997
4. Novel mutations of TGM1 in a child with congenital ichthyosiform erythroderma;Akiyama;Br J Dermatol,2001
5. Mutations of keratinocyte transglutaminase in lamellar ichthyosis;Huber;Science,1995
Cited by 15 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. Report of a Novel ALOX12B Mutation in Self-Improving Collodion Ichthyosis with an Overview of the Genetic Background of the Collodion Baby Phenotype;Life;2021-06-27
2. Unknown mutations and genotype/phenotype correlations of autosomal recessive congenital ichthyosis in patients from Saudi Arabia and Pakistan;Molecular Genetics & Genomic Medicine;2019-01
3. Ictiosis congénitas autosómicas recesivas;Actas Dermo-Sifiliográficas;2013-05
4. Autosomal Recessive Congenital Ichthyosis;Actas Dermo-Sifiliográficas (English Edition);2013-05
5. Lamellar ichthyosis with a novel homozygous C-terminal mutation in thetransglutaminase-1gene;International Journal of Dermatology;2009-11
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3