Publication | Open Access
<i>SQSTM1</i> mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
279
Citations
26
References
2012
Year
SQSTM1 mutations are present in patients with FTLD and patients with ALS. Additional studies are warranted in order to better investigate the role of p62 in the pathogenesis of both FTLD and ALS.
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