A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1–12q14. Issue 1 (5th January 2005)

Record Type:: Journal Article
Title:: A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1–12q14. Issue 1 (5th January 2005)
Main Title:: A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1–12q14
Authors:: Wilkinson, P A
Simpson, M A
Bastaki, L
Patel, H
Reed, J A
Kalidas, K
Samilchuk, E
Khan, R
Warner, T T
Crosby, A H
Abstract:
Is Part Of:: Journal of medical genetics. Volume 42:Issue 1(2005)
Journal:: Journal of medical genetics
Issue:: Volume 42:Issue 1(2005)
Issue Display:: Volume 42, Issue 1 (2005)
Year:: 2005
Volume:: 42
Issue:: 1
Issue Sort Value:: 2005-0042-0001-0000
Page Start:: 80
Page End:: 82
Publication Date:: 2005-01-05
Subjects:: HSP, hereditary spastic paraplegia
hereditary spastic paraplegia -- SPG26
Medical genetics -- Periodicals
616.042
Journal URLs:: http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jmg.2004.020172 ↗
Languages:: English
ISSNs:: 1468-6244
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:: 17950.xml