Literature DB >> 32991753

De novo novel splice-site mutation in FLT4/VEGFR3 is associated with Milroy disease.

Yuka Shibata1, Toshio Okamoto2, Takao Saruta3, Fumiya Matsuoka4, Mikiya Fujieda4, Shigetoshi Sano1.   

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Year:  2020        PMID： 32991753     DOI： 10.1111/1346-8138.15627

Source DB:  PubMed          Journal:  J Dermatol        ISSN： 0385-2407            Impact factor:   4.005


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  1 in total

1.  FLT4 Mutations Are Associated with Segmental Lymphatic Dysfunction and Initial Lymphatic Aplasia in Patients with Milroy Disease.

Authors:  Ningfei Liu; Minzhe Gao
Journal:  Genes (Basel)       Date:  2021-10-13       Impact factor: 4.096
  1 in total

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