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A novel homozygous mutation in TBK1 gene causing ALS-FTD.
Libonati, Laura; Ceccanti, Marco; Cambieri, Chiara; Colavito, Davide; Moret, Federica; Fiorini, Ilenia; Inghilleri, Maurizio.
Affiliation
  • Libonati L; Rare Neuromuscular Diseases Centre, Department of Human Neurosciences, Sapienza University, Viale dell'università 30, 00185, Rome, Italy. laura.libonati@uniroma1.it.
  • Ceccanti M; Rare Neuromuscular Diseases Centre, Department of Human Neurosciences, Sapienza University, Viale dell'università 30, 00185, Rome, Italy.
  • Cambieri C; Rare Neuromuscular Diseases Centre, Department of Human Neurosciences, Sapienza University, Viale dell'università 30, 00185, Rome, Italy.
  • Colavito D; Research & Innovation S.R.L. (R&I Genetics), 35127, Padova, Italy.
  • Moret F; Rare Neuromuscular Diseases Centre, Department of Human Neurosciences, Sapienza University, Viale dell'università 30, 00185, Rome, Italy.
  • Fiorini I; Rare Neuromuscular Diseases Centre, Department of Human Neurosciences, Sapienza University, Viale dell'università 30, 00185, Rome, Italy.
  • Inghilleri M; Rare Neuromuscular Diseases Centre, Department of Human Neurosciences, Sapienza University, Viale dell'università 30, 00185, Rome, Italy.
Neurol Sci ; 43(3): 2101-2104, 2022 Mar.
Article in En | MEDLINE | ID: mdl-35028775
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Frontotemporal Dementia / Amyotrophic Lateral Sclerosis Limits: Humans Language: En Journal: Neurol Sci Journal subject: NEUROLOGIA Year: 2022 Document type: Article Affiliation country: Country of publication:
Fulltext
Add to My VHL
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Frontotemporal Dementia / Amyotrophic Lateral Sclerosis Limits: Humans Language: En Journal: Neurol Sci Journal subject: NEUROLOGIA Year: 2022 Document type: Article Affiliation country: Country of publication: