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Brain : a Journal of Neurology|December 19, 2017
Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathiesShelley L Forrest, Jillian J Kril, Claire H Stevens, et al.
Human Molecular Genetics|May 21, 2026
Ultra-rare variants in LAMA2 are risk factors for frontotemporal dementia and motor neuron diseaseHiu Chuen Lok, Carol Dobson-Stone, Marianne Hallupp, et al.
Brain : a Journal of Neurology|July 18, 2019
Arylsulfatase A, a genetic modifier of Parkinson's disease, is an α-synuclein chaperoneJun Sung Lee, Kazuaki Kanai, Mari Suzuki, et al.
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