Literature DB >> 18279219

Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease.

Takeshi Futatani1, Eiji Nii, Makoto Obata, Fukiko Ichida, Yoshie Okabe, Hirokazu Kanegane, Toshio Miyawaki.   

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Year:  2008        PMID： 18279219     DOI： 10.1111/j.1442-200X.2007.02505.x

Source DB:  PubMed          Journal:  Pediatr Int        ISSN： 1328-8067            Impact factor:   1.524


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  1 in total

1.  Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema.

Authors:  A Mendola; M J Schlögel; A Ghalamkarpour; A Irrthum; H L Nguyen; E Fastré; A Bygum; C van der Vleuten; C Fagerberg; E Baselga; I Quere; J B Mulliken; L M Boon; P Brouillard; M Vikkula
Journal:  Mol Syndromol       Date:  2013-08-21
  1 in total

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