Exome sequencing reveals a novel ANO10 mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia. (4th April 2013)

Record Type:: Journal Article
Title:: Exome sequencing reveals a novel ANO10 mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia. (4th April 2013)
Main Title:: Exome sequencing reveals a novel ANO10 mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia
Authors:: Maruyama, H.
Morino, H.
Miyamoto, R.
Murakami, N.
Hamano, T.
Kawakami, H.
Abstract:
Is Part Of:: Clinical genetics. Volume 85:Number 3(2014:Mar.)
Journal:: Clinical genetics
Issue:: Volume 85:Number 3(2014:Mar.)
Issue Display:: Volume 85, Issue 3 (2014)
Year:: 2014
Volume:: 85
Issue:: 3
Issue Sort Value:: 2014-0085-0003-0000
Page Start:: 296
Page End:: 297
Publication Date:: 2013-04-04
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.12140 ↗
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
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Ingest File:: 3661.xml