Author | Reimann, J | dc.contributor.author |
Author | Lehmann, D | dc.contributor.author |
Author | Hardy, SA | dc.contributor.author |
Author | Falkous, G | dc.contributor.author |
Author | Knowles, CV | dc.contributor.author |
Author | Jones, RL | dc.contributor.author |
Author | Kunz, WS | dc.contributor.author |
Author | Taylor, RW | dc.contributor.author |
Author | Kornblum, C | dc.contributor.author |
Date of accession | 2019-07-25T11:53:11Z | dc.date.accessioned |
Available in OPARU since | 2019-07-25T11:53:11Z | dc.date.available |
Date of first publication | 2017 | dc.date.issued |
Publisher | Universität Ulm | dc.publisher |
Dewey Decimal Group | DDC 610 / Medicine & health | dc.subject.ddc |
Title | Camptocormia and shuffling gait due to a novel MT-TV mutation: Diagnostic pitfalls | dc.title |
Resource type | Wissenschaftlicher Artikel | dc.type |
Institution | UKU. Klinik für Neurologie | uulm.affiliationSpecific |
DCMI Type | Text | uulm.typeDCMI |
Category | Publikationsnachweise | uulm.category |
DOI (external) | 10.1212/NXG.0000000000000147 | dc.identifier.doiExternal |
Source - Title of source | Neurology Genetics | source.title |
Source - Volume | 3 | source.volume |
Source - Issue | 3 | source.issue |
Source - Year | 2017 | source.year |
Source - From page | e147 | source.fromPage |
Community | Universitätsklinikum Ulm | uulm.community |
EVALuna | 13273 | uulm.identifier.evaluna |
PubMed | 28396884 | uulm.identifier.pubmed |
Bibliography | uulm | uulm.bibliographie |