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The p.P301L mutation in microtubule‐associated protein tau (MAPT) is a common cause of frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP‐17). We compare clinicopathologic features of five unrelated and… Click to show full abstract
The p.P301L mutation in microtubule‐associated protein tau (MAPT) is a common cause of frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP‐17). We compare clinicopathologic features of five unrelated and three related (brother, sister and cousin) patients with FTDP‐17 due to p.P301L mutation.
Keywords:
associated protein;
microtubule associated;
protein tau;
tau mapt;
p301l mutation;
mutation
Journal Title: Neuropathology and Applied Neurobiology
Year Published: 2017
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Journal Title: Neuropathology and Applied Neurobiology
Year Published: 2017
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!