Novel SPG4 Mutation in a Patient with Sporadic Hereditary Spastic Paraplegia and Elevated Cerebrospinal Fluid Protein

Letter/Communication

Peer reviewed

Hongda She, Xin Zheng, Yingxiu Xiao, Frank Mastaglia, Anthony Akkari and Jingshan Wu

Journal of clinical neurology (Seoul, Korea), Vol.17(1), pp.152-153

2021

PMID: 33480217

Abstract

Clinical Neurology

Life Sciences & Biomedicine

Neurosciences & Neurology

Science & Technology

Title: Novel SPG4 Mutation in a Patient with Sporadic Hereditary Spastic Paraplegia and Elevated Cerebrospinal Fluid Protein
Authors/Creators: Hongda She - Third Affiliated Hospital of Sun Yat-sen University
Xin Zheng - Capital Medical University
Yingxiu Xiao - Shantou University
Frank Mastaglia - QE II Med Ctr, Perron Inst Neurol & Translat Sci, Nedlands, WA, Australia
Anthony Akkari - Queen Elizabeth II Jubilee Hospital
Jingshan Wu - Univ Western Australia, Fac Hlth & Med Sci, M503,35 Stirling Highway, Perth, WA 6009, Australia
Publication Details: Journal of clinical neurology (Seoul, Korea), Vol.17(1), pp.152-153
Publisher: Korean Neurological Association
Number of pages: 2
Identifiers: 991005616565507891
Copyright: © 2021 Korean Neurological Association
Murdoch Affiliation: Centre for Molecular Medicine and Innovative Therapeutics
Language: English
Resource Type: Letter/Communication

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Collaboration types: Domestic collaboration; International collaboration
Citation topics: 1 Clinical & Life Sciences; 1.52 Neurodegenerative Diseases; 1.52.951 Huntington's and Ataxias
Web Of Science research areas: Clinical Neurology
ESI research areas: Neuroscience & Behavior