AP1S2‐truncating variant in a patient with severe neurodevelopmental disorder and cerebral folate deficiency. (27th November 2018)

Record Type:: Journal Article
Title:: AP1S2‐truncating variant in a patient with severe neurodevelopmental disorder and cerebral folate deficiency. (27th November 2018)
Main Title:: AP1S2‐truncating variant in a patient with severe neurodevelopmental disorder and cerebral folate deficiency
Authors:: Cappuccio, Gerarda
Torella, Annalaura
Mastrangelo, Mario
Carducci, Claudia
Nigro, Vincenzo
Brunetti‐Pierri, Nicola
Leuzzi, Vincenzo
Abstract:
Is Part Of:: Acta pædiatrica. Volume 108:Number 3(2019)
Journal:: Acta pædiatrica
Issue:: Volume 108:Number 3(2019)
Issue Display:: Volume 108, Issue 3 (2019)
Year:: 2019
Volume:: 108
Issue:: 3
Issue Sort Value:: 2019-0108-0003-0000
Page Start:: 564
Page End:: 565
Publication Date:: 2018-11-27
Subjects:: Pediatrics -- Periodicals
Pediatrics
618.92
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1651-2227 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/apa.14633 ↗
Languages:: English
ISSNs:: 0803-5253
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 0642.400000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 23864.xml