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[Identification of VEGFR3 gene mutation in a Chinese family with autosomal dominant primary congenital lymphoedema].

Authors
Type
Published Article
Journal
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Publication Date
Volume
27
Issue
4
Pages
371–375
Identifiers
DOI: 10.3760/cma.j.issn.1003-9406.2010.04.003
PMID: 20677139
Source
Medline
License
Unknown

Abstract

This study identified a C3341T (p.Pro1114Leu) mutation in the VEGFR3 gene in a Chinese family with PCL, provided evidence that VEGFR3 mutation can cause PCL in Chinese.

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