EPHB4 kinase–inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis-Reference-Cited by-同舟云学术

EPHB4 kinase–inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis

Published:2016-07-11 Issue:8 Volume:126 Page:3080-3088
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:

Author:

Martin-Almedina Silvia,Martinez-Corral Ines,Holdhus Rita,Vicente Andres,Fotiou Elisavet,Lin Shin,Petersen Kjell,Simpson Michael A.,Hoischen Alexander,Gilissen Christian,Jeffery Heather,Atton Giles,Karapouliou Christina,Brice Glen,Gordon Kristiana,Wiseman John W.,Wedin Marianne,Rockson Stanley G.,Jeffery Steve,Mortimer Peter S.,Snyder Michael P.,Berland Siren,Mansour Sahar,Makinen Taija,Ostergaard Pia

Publisher

American Society for Clinical Investigation

Subject

General Medicine

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5. Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome

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