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Neuray, C.* ; Sultan, T.* ; Alvi, J.R.* ; Franca, M.C.* ; Assmann, B.* ; Wagner, M. ; Canafoglia, L.* ; Franceschetti, S.* ; Rossi, G.* ; Santana, I.* ; Macario, M.C.* ; Almeida, M.R.* ; Kamate, M.* ; Parikh, S.* ; Elloumi, H.Z.* ; Murphy, D.* ; Efthymiou, S.* ; Maroofian, R.* ; Houlden, H.*

Early-onset phenotype of bi-allelic GRN mutations.

Brain 144:e22 (2021)
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
ISSN (print) / ISBN 0006-8950
e-ISSN 1460-2156
Journal Brain: A Journal of Neurology
Quellenangaben Volume: 144, Issue: 2, Pages: , Article Number: e22 Supplement: ,
Publisher Oxford University Press
Publishing Place Great Clarendon St, Oxford Ox2 6dp, England
Non-patent literature Publications
Reviewing status Peer reviewed
Institute(s) Institute of Neurogenomics (ING)
Grants Muscular Dystrophy Association (MDA USA)
strategic award (Synaptopathies) funding
National Institute for Health Research University College London Hospitals Biomedical Research Centre
MRC
Rosetree Trust
Ataxia UK
MSA Trust
Brain Research UK
Sparks GOSH Charity
Muscular Dystrophy UK (MDUK)
Wellcome Trust