Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

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Acta neuropathologica - ISSN 0001-6322-128:3 (2014) p. 397-410

A Pan-European study of the **C9orf72** repeat associated with FTLD : geographic prevalence, genomic instability and intermediate repeats

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Human mutation - ISSN 1059-7794-34:2 (2013) p. 363-373
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