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

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

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Veröffentlicht in:Journal of dermatology 2021-01, Vol.48 (1), p.e26-e28
Hauptverfasser: Shibata, Yuka, Okamoto, Toshio, Saruta, Takao, Matsuoka, Fumiya, Fujieda, Mikiya, Sano, Shigetoshi
Format: Artikel
Sprache:eng
Schlagworte:
Female
Humans
Infant
Lymphedema
Mutation
Vascular Endothelial Growth Factor Receptor-3 - genetics
Vascular endothelial growth factor receptors
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creator Shibata, Yuka
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Saruta, Takao
Matsuoka, Fumiya
Fujieda, Mikiya
Sano, Shigetoshi
description
doi_str_mv 10.1111/1346-8138.15627
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Female
Humans
Infant
Lymphedema
Mutation
Vascular Endothelial Growth Factor Receptor-3 - genetics
Vascular endothelial growth factor receptors
title De novo novel splice‐site mutation in FLT4/VEGFR3 is associated with Milroy disease
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