HUWE1 mutations cause dominant XLID: a clinical and genetic study of 22 patients

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TitreHUWE1 mutations cause dominant XLID: a clinical and genetic study of 22 patients
Type de publicationJournal Article
Year of Publication2018
AuteursBerland S., Moortgat S., Aukrust I., Maystadt I., Baker L., Benoit V., Cooper N.S, Francois-Guillaume D., Faivre L., Gardeitchik T., Haukanes B.I, Houge G., Kivuva E., Mehta S., Nassogne M., Powell-Hamilton N., Pfundt R., M. Piera R, Prescott T., Vasudevan P., van Loon B., Verellen-Dumoulin C., Verloes A., von der Lippe C., Wakeling E., Wilkie A.OM, Wilson L., Yuen A.L, Newbury-Ecob R.A, Low K.J, -Study DDD
JournalEUROPEAN JOURNAL OF HUMAN GENETICS
Volume26
Pagination336-337
Date PublishedOCT
Type of ArticleMeeting Abstract
ISSN1018-4813