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Refined by: journal title: Neurology. Genetics remove
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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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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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Association study between multiple system atrophy and TREM2 p.R47H

Ogaki, Kotaro et al.

Neurology. Genetics. Volume 4:Number 4 (2018) -- [Wolters Kluwer]

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Late-onset Alzheimer disease risk variants mark brain regulatory loci

Allen, Mariet et al.

Neurology. Genetics. Volume 1:Number 2 (2015) -- [Wolters Kluwer]

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Abnormal expression of homeobox genes and transthyretin in C9ORF72 expansion carriers

Finch, NiCole A. et al.

Neurology. Genetics. Volume 3:Number 4 (2017) -- [Wolters Kluwer]

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by this Author/Contributor:

  1. Dickson, Dennis W.
  2. Graff-Radford, Neill R.
  3. Petersen, Ronald C.
  4. Heckman, Michael G.
  5. Ertekin-Taner, Nilüfer

on this subject:

  1. Neurogenetics--Periodicals

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