Portuguese family with the co-occurrence of frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis phenotypes due to progranulin gene mutation
Portuguese family with the co-occurrence of frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis phenotypes due to progranulin gene mutation
Authors
Keywords
FTLD-NCL family, Frontotemporal lobar degeneration, Neuronal ceroid lipofuscinosis, Progranulin mutation, Homozygous or heterozygous state
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