Reply to: "Autosomal‐Recessive Cerebellar Ataxias With Elevated Alpha‐Fetoprotein: Uncommon Diseases, Common Biomarker". Issue 3 (22nd March 2021)

Record Type:: Journal Article
Title:: Reply to: "Autosomal‐Recessive Cerebellar Ataxias With Elevated Alpha‐Fetoprotein: Uncommon Diseases, Common Biomarker". Issue 3 (22nd March 2021)
Main Title:: Reply to: "Autosomal‐Recessive Cerebellar Ataxias With Elevated Alpha‐Fetoprotein: Uncommon Diseases, Common Biomarker"
Authors:: Renaud, Mathilde
Tranchant, Christine
Koenig, Michel
Anheim, Mathieu
Abstract:
Is Part Of:: Movement disorders. Volume 36:Issue 3(2021)
Journal:: Movement disorders
Issue:: Volume 36:Issue 3(2021)
Issue Display:: Volume 36, Issue 3 (2021)
Year:: 2021
Volume:: 36
Issue:: 3
Issue Sort Value:: 2021-0036-0003-0000
Page Start:: 789
Page End:: 790
Publication Date:: 2021-03-22
Subjects:: recessive ataxia -- alpha‐fetoprotein -- oculomotor apraxia -- DNA/RNA repair
Movement disorders -- Periodicals
610
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1531-8257 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/mds.28524 ↗
Languages:: English
ISSNs:: 0885-3185
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 5980.317200
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 16564.xml