A large multiexonic genomic deletion within the ALMS1 gene causes Alström syndrome in a consanguineous Pakistani family. Issue 4 (18th August 2015)

Record Type:: Journal Article
Title:: A large multiexonic genomic deletion within the ALMS1 gene causes Alström syndrome in a consanguineous Pakistani family. Issue 4 (18th August 2015)
Main Title:: A large multiexonic genomic deletion within the ALMS1 gene causes Alström syndrome in a consanguineous Pakistani family
Authors:: Nikopoulos, K.
Butt, G. U.
Farinelli, P.
Mudassar, M.
Domènech‐Estévez, E.
Samara, C.
Kausar, M.
Masroor, I.
Chrast, R.
Rivolta, C.
Siddiqi, S.
Abstract:
Is Part Of:: Clinical genetics. Volume 89:Issue 4(2016)
Journal:: Clinical genetics
Issue:: Volume 89:Issue 4(2016)
Issue Display:: Volume 89, Issue 4 (2016)
Year:: 2016
Volume:: 89
Issue:: 4
Issue Sort Value:: 2016-0089-0004-0000
Page Start:: 510
Page End:: 511
Publication Date:: 2015-08-18
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.12645 ↗
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:: 1224.xml