Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy’s disease
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.2007.02505.x/fullpdf
Reference9 articles.
1. Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema
2. Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase
3. Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema
Cited by 5 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. A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects;European Journal of Medical Research;2022-12-10
2. De novo novel splice‐site mutation in FLT4/VEGFR3 is associated with Milroy disease;The Journal of Dermatology;2020-09-29
3. Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema;Molecular Syndromology;2013
4. FLT4/VEGFR3and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update;Human Mutation;2012-10-16
5. Recessive primary congenital lymphoedema caused by a VEGFR3 mutation;Journal of Medical Genetics;2009-03-15
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