Motor function decline correlates with behavioral impairment in C9orf72 mutation carriers

Neurology. 2020 Jan 21;94(3):134-136. doi: 10.1212/WNL.0000000000008810. Epub 2019 Dec 17.

Authors

Shreya Gandhy¹, Jennifer Farren¹, Mary Kay Floeter²

Affiliations

¹ From the National Institute of Neurological Disorders and Stroke (J.F., M.K.F.), National Institutes of Health, Bethesda, MD, and Department of Neurology (S.G.), George Washington University, Washington, DC.
² From the National Institute of Neurological Disorders and Stroke (J.F., M.K.F.), National Institutes of Health, Bethesda, MD, and Department of Neurology (S.G.), George Washington University, Washington, DC. [email protected].

No abstract available

MeSH terms

Aged
Amyotrophic Lateral Sclerosis / complications*
Amyotrophic Lateral Sclerosis / genetics
Amyotrophic Lateral Sclerosis / psychology
C9orf72 Protein / genetics*
Female
Frontotemporal Dementia / complications*
Frontotemporal Dementia / genetics
Frontotemporal Dementia / psychology
Heterozygote
Humans
Male
Mental Disorders / etiology*
Middle Aged
Motor Activity*
Mutation

Substances

C9orf72 Protein
C9orf72 protein, human

Supplementary concepts

Frontotemporal Dementia With Motor Neuron Disease

Grants and funding

ZIA NS003146/ImNIH/Intramural NIH HHS/United States