Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease.
Identifieur interne : 002F17 ( PubMed/Checkpoint ); précédent : 002F16; suivant : 002F18Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease.
Auteurs : Takeshi Futatani [Japon] ; Eiji Nii ; Makoto Obata ; Fukiko Ichida ; Yoshie Okabe ; Hirokazu Kanegane ; Toshio MiyawakiSource :
- Pediatrics international : official journal of the Japan Pediatric Society [ 1328-8067 ] ; 2008.
Descripteurs français
- KwdFr :
- MESH :
- Wicri :
- geographic : Japon.
English descriptors
- KwdEn :
- MESH :
- chemical , analysis : DNA, Complementary.
- chemical , genetics : Vascular Endothelial Growth Factor Receptor-3.
- geographic : Japan.
- genetics : Asian Continental Ancestry Group, Lymphedema.
- Female, Humans, Infant, Infant, Newborn, Male, Mutation, Mutation, Missense, Pedigree.
DOI: 10.1111/j.1442-200X.2007.02505.x
PubMed: 18279219
Affiliations:
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pubmed:18279219Le document en format XML
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<term>Mâle</term>
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<Title>Pediatrics international : official journal of the Japan Pediatric Society</Title>
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<ArticleTitle>Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease.</ArticleTitle>
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<name sortKey="Obata, Makoto" sort="Obata, Makoto" uniqKey="Obata M" first="Makoto" last="Obata">Makoto Obata</name>
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<country name="Japon"><noRegion><name sortKey="Futatani, Takeshi" sort="Futatani, Takeshi" uniqKey="Futatani T" first="Takeshi" last="Futatani">Takeshi Futatani</name>
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