Hereditary defect of cobalamin metabolism (homocystinuria and methylmalonic aciduria) of juvenile onset. Issue 1 (January 1996)

Record Type:: Journal Article
Title:: Hereditary defect of cobalamin metabolism (homocystinuria and methylmalonic aciduria) of juvenile onset. Issue 1 (January 1996)
Main Title:: Hereditary defect of cobalamin metabolism (homocystinuria and methylmalonic aciduria) of juvenile onset.
Authors:: Gold, R
Bogdahn, U
Kappos, L
Toyka, K V
Baumgartner, E R
Fowler, B
Wendel, U
Abstract:
Is Part Of:: Journal of neurology, neurosurgery and psychiatry. Volume 60:Issue 1(1996)
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 60:Issue 1(1996)
Issue Display:: Volume 60, Issue 1 (1996)
Year:: 1996
Volume:: 60
Issue:: 1
Issue Sort Value:: 1996-0060-0001-0000
Page Start:: 107
Page End:: 108
Publication Date:: 1996-01
Subjects:: Neurology -- Periodicals
Nervous system -- Surgery -- Periodicals
Psychiatry -- Periodicals
616.8
Journal URLs:: http://jnnp.bmjjournals.com/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?action=archive&journal=192 ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jnnp.60.1.107 ↗
Languages:: English
ISSNs:: 0022-3050
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - BLDSS-3PM
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Ingest File:: 23647.xml