首页> Movement disorders clinical practice> Expanding <i>MAPT</i> p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophy.

Expanding <i>MAPT</i> p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophy.

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第一作者： Jacy Bezerra,Parmera

第一单位： Department of Neurology, Hospital das Clínicas Faculdade de Medicina da Universidade de São Paulo (HC-FMUSP) São Paulo Brazil.

作者： Jacy Bezerra,Parmera ^[1] ; Artur Martins,Coutinho ^[2] ; Thiago Gonçalves,Guimarães ^[1] ; Joyce,Yuri Silvestre Yamamoto ^[1] ; Leonel Tadao,Takada ^[1] ; Ricardo,Nitrini ^[1] ; Egberto Reis,Barbosa ^[1] ; Sonia Maria Dozzi,Brucki ^[1]

作者单位： Department of Neurology, Hospital das Clínicas Faculdade de Medicina da Universidade de São Paulo (HC-FMUSP) São Paulo Brazil. ^[1] Laboratory of Nuclear Medicine (LIM 43), Nuclear Medicine Center, Institute of Radiology, Hospital das Clínicas Faculdade de Medicina da Universidade de São Paulo (HC-FMUSP) São Paulo Brazil. ^[2]

关键词 MAPT gene corticobasal degeneration corticobasal syndrome frontotemporal lobar degeneration progressive supranuclear palsy

DOI 10.1002/mdc3.13671

PMID 37070053

发布时间 2024-02-15

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Movement disorders clinical practice

2023年10卷4期

716-718页

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Movement disorders clinical practice

2023年10卷4期

716-718页

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Expanding <i>MAPT</i> p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophy.

Movement disorders clinical practice

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Movement disorders clinical practice

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Expanding <i>MAPT</i> p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophy.

Movement disorders clinical practice

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Movement disorders clinical practice

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