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Kjellin syndrome: hereditary spastic paraplegia with pathognomonic macular appearance. (2014)

First Author: Nowak VA

Attributed to: Using Next Generation Sequencing to Unravel the Pathogenesis of Sporadic Inclusion Body Myositis - The International IBM Consortium Genetic Study funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/practneurol-2014-000861

PubMed Identifier: 24924740

Publication URI: http://europepmc.org/abstract/MED/24924740

Type: Journal Article/Review

Volume: 14

Parent Publication: Practical neurology

Issue: 4

ISSN: 1474-7758