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dc.contributor.author | Soehn, Anne S. |
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dc.contributor.author | Rattay, Tim W. |
dc.contributor.author | Beck-Wödl, Stefanie |
dc.contributor.author | Schäferhoff, Karin |
dc.contributor.author | Monk, Dave Nicholas |
dc.contributor.author | Döbler-Neumann, Marion |
dc.contributor.author | Hörtnagel, Konstanze |
dc.contributor.author | Schlüter, Agatha |
dc.contributor.author | Ruiz, Montserrat |
dc.contributor.author | Pujol Onofre, Aurora |
dc.contributor.author | Züchner, Stephan |
dc.contributor.author | Riess, Olaf |
dc.contributor.author | Schüle, Rebecca |
dc.contributor.author | Bauer, Peter |
dc.contributor.author | Schöls, Ludger |
dc.date | 2018-12-10T12:01:17Z |
dc.date | 2018-12-10T12:01:17Z |
dc.date | 2016-07-12 |
dc.date | 2018-07-25T07:46:55Z |
dc.identifier.uri | http://hdl.handle.net/2445/126828 |
dc.format | 6 p. |
dc.format | application/pdf |
dc.language.iso | eng |
dc.publisher | Lippincott Williams & Wilkins |
dc.relation | Reproducció del document publicat a: https://doi.org/10.1212/WNL.0000000000002843 |
dc.relation | Neurology, 2016, vol. 87, num. 2, p. 186-191 |
dc.relation | https://doi.org/10.1212/WNL.0000000000002843 |
dc.rights | (c) American Academy of Neurology, 2016 |
dc.rights | info:eu-repo/semantics/openAccess |
dc.subject | Paraplegia |
dc.subject | Malalties hereditàries |
dc.subject | Genetic disorders |
dc.title | Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families |
dc.type | info:eu-repo/semantics/article |
dc.type | info:eu-repo/semantics/publishedVersion |
dc.description.abstract |