Updated insight into the mutational and phenotypic spectrum of MED13L-related intellectual disability

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TitreUpdated insight into the mutational and phenotypic spectrum of MED13L-related intellectual disability
Type de publicationJournal Article
Year of Publication2020
AuteursAsadollahi R., Boonsawat P., Popp B., Torti E., Bader I., Vitobello A., Moutton S., Pinson L., Lambert L., Thuresson A.C, Sobol M., C. Zander S, Platzer K., Strehlow V., Hornemann F., Zacher P., F. Mau-Them T, Bruel A.L, Hajianpour M.J, Kovacs-Nagy R., Lay-Son G., Amlie-Wolf L., Kaplan J., Chassevent A., Smith-Hicks C., Slavotinek A., Kukolich M.K, Nugent K., Roeder E., Zarate Y.A, Toshiyuki Y., Jackel-Cram C., Maystadt I., Mehta S.G, Briggs T.A, Chandler K., van Haeringen A., Kraus C., Zweier C., Reis A., Rauch A.
JournalEUROPEAN JOURNAL OF HUMAN GENETICS
Volume28
Pagination350-351
Date PublishedDEC
Type of ArticleMeeting Abstract
ISSN1018-4813