ExLibris header image
SFX Logo
Title: KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia
Source:

European Journal of Human Genetics [1018-4813] Pennings, Maartje yr:2019


Collapse list of basic services Basic
Full text
Full text available via Nature
GO
Full text available via PubMed Central
GO
Document delivery
Request document via Library/Bibliothek GO

Expand list of advanced services Advanced
A service provided by the Library of the Wissenschaftspark Albert Einstein, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.