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Hereditary spastic paraplegia in Greece: characterisation of a previously unexplored population using next-generation sequencing. (2016)

First Author: Lynch DS

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/10.1038/ejhg.2015.200

PubMed Identifier: 26374131

Publication URI: http://europepmc.org/abstract/MED/26374131

Type: Journal Article/Review

Volume: 24

Parent Publication: European journal of human genetics : EJHG

Issue: 6

ISSN: 1018-4813