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Identification ofUBAP1mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project
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William Harvey Research Institute
Centre for Clinical Pharmacology
Identification ofUBAP1mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project
QMRO Home
William Harvey Research Institute
Centre for Clinical Pharmacology
Identification ofUBAP1mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project
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Identification ofUBAP1mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project
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Accepted version (60.18Kb)
DOI
10.1038/s41431-020-00720-w
Journal
EUROPEAN JOURNAL OF HUMAN GENETICS
ISSN
1018-4813
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Authors
Bourinaris, T; Smedley, D; Cipriani, V; Sheikh, I; Athanasiou-Fragkouli, A; Chinnery, P; Morris, H; Real, R; Harrison, V; Reid, E
URI
https://qmro.qmul.ac.uk/xmlui/handle/123456789/67071
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Centre for Clinical Pharmacology
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