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pubmed-article:18779421pubmed:abstractTextAbnormal neuronal inclusions composed of the transactivation response DNA-binding protein 43 (TDP-43) are characteristic neuropathologic lesions in sporadic and familial forms of amyotrophic lateral sclerosis (ALS). This makes TARDBP, the gene encoding for TDP-43, a candidate for genetic screening in ALS.lld:pubmed
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pubmed-article:18779421pubmed:articleTitleTwo German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations.lld:pubmed
pubmed-article:18779421pubmed:affiliationCenter for Neuropathology and Prion Research, Ludwig-Maximilians University, Munich, Feodor-Lynen-Strasse 23, 81377 Munich, Germany.lld:pubmed
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