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Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 gene

Crossref DOI link: https://doi.org/10.1016/j.nmd.2016.10.001

Published Print: 2017-01

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Rossor, Alexander M.

Morrow, Jasper M.

Polke, James M.

Murphy, Sinead M.

Houlden, Henry

Laura, Matilde

Manji, Hadi

Blake, Julian

Reilly, Mary M.
Funding

Funding for this research was provided by:

Wellcome Trust Postdoctoral Research Training Fellowship for Clinicians (110043/Z/15/Z)

National Institutes of Neurological Diseases and Stroke and Office of Rare Diseases (U54NS065712)

Medical Research Council (G0601943)

National Institute for Health Research University College London Hospitals Biomedical Research Centre
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Text and Data Mining valid from 2017-01-01

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This article is maintained by: Elsevier

Article Title: Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 gene

Journal Title: Neuromuscular Disorders

CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.nmd.2016.10.001

Content Type: article

Copyright: © 2016 The Authors. Published by Elsevier B.V.