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O
Olszewska, DA;
Fearon, C;
McGuigan, C;
McVeigh, TP;
Houlden, H;
Polke, JM;
Lawlor, B;
... Lynch, T; + view all
(2021)
A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene.
Neurobiology of Aging
, 106
343.e1-343.e8.
10.1016/j.neurobiolaging.2021.05.010.
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