Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families. (February 2018)

Record Type:: Journal Article
Title:: Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families. (February 2018)
Main Title:: Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families
Authors:: Kocoglu, Cemile
Gundogdu, Asli
Kocaman, Gulsen
Kahraman-Koytak, Pinar
Uluc, Kayihan
Kiziltan, Gunes
Caglayan, Ahmet Okay
Bilguvar, Kaya
Vural, Atay
Basak, A. Nazli
Abstract:
Is Part Of:: Neurology. Volume 4:Number 1(2018)
Journal:: Neurology
Issue:: Volume 4:Number 1(2018)
Issue Display:: Volume 4, Issue 1 (2018)
Year:: 2018
Volume:: 4
Issue:: 1
Issue Sort Value:: 2018-0004-0001-0000
Page Start:
Page End:
Publication Date:: 2018-02
Subjects:: Neurogenetics -- Periodicals
616.80442
Journal URLs:: http://ng.neurology.org/ ↗
http://journals.lww.com/pages/default.aspx ↗
DOI:: 10.1212/NXG.0000000000000218 ↗
Languages:: English
ISSNs:: 2376-7839
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 6317.xml