Novel homozygous mutation in exon 5 of WFS1 gene in an Apulian family with mild phenotypic expression of Wolfram syndrome. (3rd October 2013)

Record Type:: Journal Article
Title:: Novel homozygous mutation in exon 5 of WFS1 gene in an Apulian family with mild phenotypic expression of Wolfram syndrome. (3rd October 2013)
Main Title:: Novel homozygous mutation in exon 5 of WFS1 gene in an Apulian family with mild phenotypic expression of Wolfram syndrome
Authors:: Piccinno, E.
Ortolani, F.
Vendemiale, M.
Tummolo, A.
Masciopinto, M.
Natale, M.P.
De Luca, A.
Agolini, E.
Aloi, C.
Salina, A.
D'Annunzio, G.
Fischetto, R.
Papadia, F.
Abstract:
Is Part Of:: Clinical genetics. Volume 86:Number 2(2014:Aug.)
Journal:: Clinical genetics
Issue:: Volume 86:Number 2(2014:Aug.)
Issue Display:: Volume 86, Issue 2 (2014)
Year:: 2014
Volume:: 86
Issue:: 2
Issue Sort Value:: 2014-0086-0002-0000
Page Start:: 197
Page End:: 198
Publication Date:: 2013-10-03
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.12260 ↗
Languages:: English
ISSNs:: 0009-9163
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3286.287000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 4361.xml