Loss of ADAMTS3 activity causes Hennekam lymphangiectasia–lymphedema syndrome 3-Reference-Cited by-同舟云学术

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Loss of ADAMTS3 activity causes Hennekam lymphangiectasia–lymphedema syndrome 3

Published:2017-08-02 Issue:21 Volume:26 Page:4095-4104
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Brouillard Pascal,Dupont Laura,Helaers Raphael,Coulie Richard,Tiller George E,Peeden Joseph,Colige Alain,Vikkula Miikka

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/26/21/4095/21359630/ddx297.pdf

Reference27 articles.

1. Genetics of lymphatic anomalies;J. Clin. Invest,2014

2. A novel mutation in CELSR1 is associated with hereditary lymphedema;Vasc. Cell,2016

3. EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis;J. Clin. Invest,2016

4. Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome;Hum. Genet,2014

5. Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis;Nat. Commun,2015

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