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Rare novel CYP2U1 and ZFYVE26 variants identified in two Pakistani families with spastic paraplegia. (2020)

First Author: Bibi F

Attributed to: Leveraging the power of genomics and transcriptomics to revolutionise the diagnosis and understanding of neurological disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.jns.2020.116669

PubMed Identifier: 32006740

Publication URI: http://europepmc.org/abstract/MED/32006740

Type: Journal Article/Review

Volume: 411

Parent Publication: Journal of the neurological sciences

ISSN: 0022-510X