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

Jacy Bezerra Parmera,Artur Martins Coutinho,Thiago Gonçalves Guimarães, Joyce Yuri Silvestre Yamamoto,Leonel Tadao Takada,Ricardo Nitrini,Egberto Reis Barbosa,Sonia Maria Dozzi Brucki

Movement disorders clinical practice（2023）

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摘要

Figure S1. Pedigree chart. Appendix S1. Supporting information. Appendix S2. Supporting information. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

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关键词

MAPT gene,corticobasal degeneration,corticobasal syndrome,frontotemporal lobar degeneration,progressive supranuclear palsy

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