Associated Papers
Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database.
Tunca C et al.
Human Mutation, 2020
Key role of UBQLN2 in pathogenesis of amyotrophic lateral sclerosis and frontotemporal dementia.
Renaud L et al.
Acta Neuropathologica Communications, 2019
The distinct genetic pattern of ALS in Turkey and novel mutations.
Özoğuz A et al.
Neurobiology of Aging, 2015
The changing scene of amyotrophic lateral sclerosis.
Robberecht W et al.
Nature Reviews. Neuroscience, 2013
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.
Deng HX et al.
Nature, 2011
21857683 (PubMed )
Supplement: NIHMS313102-supplement-1.pdf
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