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Journal of Neurology
Published in: Journal of Neurology 6/2016

01-06-2016 | Letter to the Editors

Triple trouble: a striking new phenotype or competing genes in a family with hereditary spastic paraplegia

Authors: Viorica Chelban, David S. Lynch, Henry Houlden, Nick Wood

Published in: Journal of Neurology | Issue 6/2016

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Excerpt

Dear Sirs, …
Literature
1.
Solowska JM, Baas PW (2015) Hereditary spastic paraplegia SPG4: what is known and not known about the disease. Brain 138:2471–2484CrossRefPubMed
2.
Pfeffer G et al (2014) Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance. Brain 137:1323–1336CrossRefPubMedPubMedCentral
3.
(1988) National Institutes of Health Consensus Development Conference Statement: neurofibromatosis. Bethesda, Md., USA, July 13–15, 1987. Neurofibromatosis 1:172–8
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Hilliard AA, Weinberger SE, Tierney LM Jr, Midthun DE, Saint S (2004) Clinical problem-solving. Occam’s razor versus Saint’s Triad. N Engl J Med 350:599–603CrossRefPubMed
Metadata
Title
Triple trouble: a striking new phenotype or competing genes in a family with hereditary spastic paraplegia
Authors
Viorica Chelban
David S. Lynch
Henry Houlden
Nick Wood
Publication date
01-06-2016
Publisher
Springer Berlin Heidelberg
Published in
Journal of Neurology / Issue 6/2016
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-016-8103-6

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