Novel splice site mutation in EIF2AK3 gene causes Wolcott‐Rallison syndrome in a consanguineous family from Saudi Arabia. (29th March 2017)

Record Type:: Journal Article
Title:: Novel splice site mutation in EIF2AK3 gene causes Wolcott‐Rallison syndrome in a consanguineous family from Saudi Arabia. (29th March 2017)
Main Title:: Novel splice site mutation in EIF2AK3 gene causes Wolcott‐Rallison syndrome in a consanguineous family from Saudi Arabia
Authors:: Al‐Aama, Jumana Yousuf
Al‐Zahrani, Hams Saeed
Jelani, Musharraf
Sabir, Hesham Salih
Al‐Saeedi, Saad Abdullah
Ahmed, Saleem
Abstract:
Is Part Of:: Congenital anomalies. Volume 58:Number 1(2018)
Journal:: Congenital anomalies
Issue:: Volume 58:Number 1(2018)
Issue Display:: Volume 58, Issue 1 (2018)
Year:: 2018
Volume:: 58
Issue:: 1
Issue Sort Value:: 2018-0058-0001-0000
Page Start:: 39
Page End:: 40
Publication Date:: 2017-03-29
Subjects:: Abnormalities, Human -- Periodicals
616.043
Journal URLs:: http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/loi/cga ↗
DOI:: 10.1111/cga.12217 ↗
Languages:: English
ISSNs:: 0914-3505
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3410.683000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 5696.xml