Human Genome Epidemiology Literature Finder
Rare Diseases
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Query Trace: Gerstmann Syndrome[original query] |
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An autopsy case of type A FTLD-TDP with a GRN mutation presenting with the logopenic variant of primary progressive aphasia at onset and with corticobasal syndrome subsequently. Neuropathology : official journal of the Japanese Society of Neuropathology 2024 5 . Takafumi Tomenaga, Shinobu Minatani, Hiroto Namba, Akitoshi Takeda, Takahito Yoshizaki, Joji Kawabe, Nazere Keyoumu, Hiroyuki Morino, Makoto Higuchi, Tomoyasu Matsubara, Hiroyuki Hatsuta, Masato Hasegawa, Shigeo Murayama, Yoshiaki It |
- Page last reviewed:Feb 1, 2024
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