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A novel HTRA1 exon 2 mutation causes loss of protease activity in a Pakistani CARASIL patient. (2015)

First Author: Khaleeli Z

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/10.1007/s00415-015-7769-5

PubMed Identifier: 25957642

Publication URI: http://europepmc.org/abstract/MED/25957642

Type: Journal Article/Review

Volume: 262

Parent Publication: Journal of neurology

Issue: 5

ISSN: 0340-5354