PUM1 haploinsufficiency is associated with syndromic neurodevelopmental delay and epilepsy. Issue 3 (20th December 2019)

Record Type:: Journal Article
Title:: PUM1 haploinsufficiency is associated with syndromic neurodevelopmental delay and epilepsy. Issue 3 (20th December 2019)
Main Title:: PUM1 haploinsufficiency is associated with syndromic neurodevelopmental delay and epilepsy
Authors:: Voet, Julie
Ceulemans, Berten
Kooy, Frank
Meuwissen, Marije E. C.
Abstract:
Is Part Of:: American journal of medical genetics. Volume 182:Issue 3(2020)
Journal:: American journal of medical genetics
Issue:: Volume 182:Issue 3(2020)
Issue Display:: Volume 182, Issue 3 (2020)
Year:: 2020
Volume:: 182
Issue:: 3
Issue Sort Value:: 2020-0182-0003-0000
Page Start:: 591
Page End:: 594
Publication Date:: 2019-12-20
Subjects:: Medical genetics -- Periodicals
616.14205
Journal URLs:: http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/ajmg.a.61463 ↗
Languages:: English
ISSNs:: 1552-4825
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 0827.920000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 12801.xml