A Novel Mutation (D395A) in Valosin-Containing Protein Gene Is Associated With Early Onset Frontotemporal Dementia in an Italian Family.

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第一作者： Francesco,Bruno

第一单位： Regional Neurogenetic Centre (CRN), Department of Primary Care, ASP Catanzaro, Lamezia Terme, Italy.

作者： Francesco,Bruno ^[1] ; Maria Elena,Conidi ^[2] ; Gianfranco,Puccio ^[1] ; Francesca,Frangipane ^[1] ; Valentina,Laganà ^[1] ; Livia,Bernardi ^[1] ; Nicoletta,Smirne ^[1] ; Maria,Mirabelli ^[1] ; Rosanna,Colao ^[1] ; Sabrina,Curcio ^[1] ; Raffaele,Di Lorenzo ^[1] ; Raffaele,Maletta ^[1] ; Amalia Cecilia,Bruni ^[1]

作者单位： Regional Neurogenetic Centre (CRN), Department of Primary Care, ASP Catanzaro, Lamezia Terme, Italy. ^[1] Laboratorio Analisi Dell'Ospedale G. Jazzolino-ASP Vibo Valentia (RC), Reggio Calabria, Italy. ^[2]

关键词 D395A Paget’s disease of bone VCP gene Valosin-Containing Protein body myopathy bvFTD frontotemporal dementia novel mutation

DOI 10.3389/fgene.2021.795029

PMID 34917136

发布时间 2021-12-18

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Frontiers in genetics

2021年12卷

795029页

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A Novel Mutation (D395A) in Valosin-Containing Protein Gene Is Associated With Early Onset Frontotemporal Dementia in an Italian Family.

Frontiers in genetics

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Frontiers in genetics

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A Novel Mutation (D395A) in Valosin-Containing Protein Gene Is Associated With Early Onset Frontotemporal Dementia in an Italian Family.

Frontiers in genetics

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Frontiers in genetics

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