Valosin-containing protein Asp395Gly mutation in a patient with frontotemporal dementia: a case report

BACKGROUND: Variants in the valosin-containing protein (VCP) gene were identified as one of the causes for inclusion body myopathy associated with Paget disease of the bone and frontotemporal dementia (FTD). Previously identified pathogenic variants in VCP are associated with frontotemporal lobar de...

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Detalles Bibliográficos
Autores principales: Kobayashi, Ryota, Naruse, Hiroya, Kawakatsu, Shinobu, Iseki, Chifumi, Suzuki, Yuya, Koyama, Shingo, Morioka, Daichi, Ishiura, Hiroyuki, Mitsui, Jun, Ohta, Yasuyuki, Tsuji, Shoji, Toda, Tatsushi, Otani, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9632072/
https://www.ncbi.nlm.nih.gov/pubmed/36329418
http://dx.doi.org/10.1186/s12883-022-02951-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9632072/
https://www.ncbi.nlm.nih.gov/pubmed/36329418
http://dx.doi.org/10.1186/s12883-022-02951-4

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