Characterizing the Clinical Features and Atrophy Patterns of <i>MAPT</i> -Related Frontotemporal Dementia With Disease Progression Modeling
<h3>Background and Objective</h3> Mutations in the <i>MAPT</i> gene cause frontotemporal dementia (FTD). Most previous studies investigating the neuroanatomical signature of <i>MAPT</i> mutations have grouped all different mutations together and shown an associati...
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Format: | Artigo |
Language: | English |
Published: |
2021
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Online Access: | https://doi.org/10.1212/wnl.0000000000012410 https://n.neurology.org/content/neurology/97/9/e941.full.pdf |
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