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Expert commentary for fragile X premutation mimicking late onset hereditary spastic paraplegia.
Rudaks, Laura Ivete; Yeow, Dennis; Kumar, Kishore Raj.
Affiliation
  • Rudaks LI; Translational Neurogenomics Group, Concord Repatriation General Hospital, Hospital Rd, Concord, NSW, 2139, Australia; Molecular Medicine Laboratory and Neurology Department, Concord Repatriation General Hospital, Hospital Rd, Concord, NSW, 2139, Australia; The University of Sydney, Camperdown, NSW, 2050, Australia; Genomic and Inherited Disease Program, The Garvan Institute of Medical Research, 384 Victoria St, Darlinghurst, NSW, 2010, Australia; Clinical Genetics Unit, Royal North Shore Hospita
  • Yeow D; Translational Neurogenomics Group, Concord Repatriation General Hospital, Hospital Rd, Concord, NSW, 2139, Australia; Molecular Medicine Laboratory and Neurology Department, Concord Repatriation General Hospital, Hospital Rd, Concord, NSW, 2139, Australia; The University of Sydney, Camperdown, NSW, 2050, Australia; Genomic and Inherited Disease Program, The Garvan Institute of Medical Research, 384 Victoria St, Darlinghurst, NSW, 2010, Australia; Neurodegenerative Service, Prince of Wales Hospit
  • Kumar KR; Translational Neurogenomics Group, Concord Repatriation General Hospital, Hospital Rd, Concord, NSW, 2139, Australia; Molecular Medicine Laboratory and Neurology Department, Concord Repatriation General Hospital, Hospital Rd, Concord, NSW, 2139, Australia; The University of Sydney, Camperdown, NSW, 2050, Australia; Genomic and Inherited Disease Program, The Garvan Institute of Medical Research, 384 Victoria St, Darlinghurst, NSW, 2010, Australia; St Vincent's Healthcare Campus, Faculty of Medici
Parkinsonism Relat Disord ; 119: 105969, 2024 Feb.
Article in En | MEDLINE | ID: mdl-38155044
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spastic Paraplegia, Hereditary / Fragile X Syndrome Limits: Humans Language: En Journal: Parkinsonism Relat Disord Journal subject: NEUROLOGIA Year: 2024 Document type: Article
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spastic Paraplegia, Hereditary / Fragile X Syndrome Limits: Humans Language: En Journal: Parkinsonism Relat Disord Journal subject: NEUROLOGIA Year: 2024 Document type: Article