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A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: possible correlation with poor response to fetal therapy

Identifieur interne : 001205 ( Istex/Checkpoint ); précédent : 001204; suivant : 001206

A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: possible correlation with poor response to fetal therapy

Auteurs : Gwo-Chin Ma [Taïwan] ; Chin-San Liu [Taïwan] ; Shun-Ping Chang [Taïwan] ; Kun-Tu Yeh [Taïwan] ; Yu-Yuan Ke [Taïwan] ; Tze-Ho Chen [Taïwan] ; Boris Bao-Tyan Wang [Taïwan, États-Unis] ; Shou-Jen Kuo [Taïwan] ; Jin-Chung Shih [Taïwan] ; Ming Chen [Taïwan, République populaire de Chine]

Source :

RBID : ISTEX:E53D47EB3307AC12FF92628361CA0983E69705EF

Abstract

To assess the possible correlations between the reported candidate genes (VEGFR3, FOXC2, ITGA9 and ITGB1) and the clinical response in fetuses with severe congenital chylothorax (CC) treated by prenatal OK‐432 pleurodesis.

Url:
DOI: 10.1002/pd.2130


Affiliations:


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ISTEX:E53D47EB3307AC12FF92628361CA0983E69705EF

Le document en format XML

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