(Q39883397)
Statements
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Portuguese family with the co-occurrence of frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis phenotypes due to progranulin gene mutation (English)
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Maria C Macário
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Lina Ramos
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Maria H Ribeiro
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Isabel Santana
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3 March 2016
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41
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200.e1-200.e5
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Identifiers
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