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Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia

van Blitterswijk, Marka et al.

Amyotrophic lateral sclerosis and frontotemporal degeneration. Volume 14:Issue 5/6 (2013); pp 463-469 -- Informa Healthcare

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ABCA7 loss-of-function variants, expression, and neurologic disease risk

Allen, Mariet et al.

Neurology -- [Wolters Kluwer] -- Volume: 3 1; -- 2017

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Polysomnographic Findings in Dementia With Lewy Bodies

Pao, Winnie C. et al.

The neurologist. Volume 19:Issue 1 (2015, January) -- Lippincott Williams & Wilkins

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ABCA7 loss-of-function variants, expression, and neurologic disease risk

Allen, Mariet et al.

Neurology. Genetics. Volume 3:Number 1 (2017) -- [Wolters Kluwer]

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APOE ε4 is associated with severity of Lewy body pathology independent of Alzheimer pathology

Dickson, Dennis W. et al.

Neurology. Volume 91:Number 12 (2018) -- Lippincott Williams & Wilkins

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RAB39B gene mutations are not a common cause of Parkinson's disease or dementia with Lewy bodies

Hodges, Kyndall et al.

NEUROBIOLOGY OF AGING. Volume 45 (2016); pp 107-108

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MAPT haplotype diversity in multiple system atrophy

Labbé, Catherine et al.

Parkinsonism & related disorders. Volume 30 (2016); pp 40-45 -- Elsevier

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TREM2 p.R47H substitution is not associated with dementia with Lewy bodies

Walton, Ronald L. et al.

Neurology. Genetics. Volume 2:Number 4 (2016) -- [Wolters Kluwer]

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MAPT haplotype H1G is associated with increased risk of dementia with Lewy bodies

Labbé, Catherine et al.

Alzheimer's & dementia: the journal of the Alzheimer's Association. Volume 12:Issue 12 (2016); pp 1297-1304 -- Elsevier

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Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders

Ogaki, Kotaro et al.

Neurology. Volume 85:Number 23 (2015, December 11th) -- Lippincott Williams & Wilkins

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