GJC2 Missense Mutations Cause Human Lymphedema-Reference-Cited by-同舟云学术

GJC2 Missense Mutations Cause Human Lymphedema

Published:2010-06 Issue:6 Volume:86 Page:943-948
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ferrell Robert E.,Baty Catherine J.,Kimak Mark A.,Karlsson Jenny M.,Lawrence Elizabeth C.,Franke-Snyder Marlise,Meriney Stephen D.,Feingold Eleanor,Finegold David N.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference30 articles.

1. Lymphedema;Kobayashi;Clin. Plast. Surg.,1987

2. Estimating the population burden of lymphedema;Rockson;Ann. N Y Acad. Sci.,2008

3. Hereditary lymphedema: evidence for linkage and genetic heterogeneity;Ferrell;Hum. Mol. Genet.,1998

4. Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema;Karkkainen;Nat. Genet.,2000

5. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome;Fang;Am. J. Hum. Genet.,2000

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