dc.contributor.author |
Röben, Benjamin |
|
dc.contributor.author |
Ruf, Susanne |
|
dc.contributor.author |
Bender, Benjamin |
|
dc.contributor.author |
Benkert, Tanja |
|
dc.contributor.author |
Reich, Selina |
|
dc.contributor.author |
Synofzik, Matthis |
|
dc.contributor.author |
Schüle-Freyer, Rebecca |
|
dc.contributor.author |
Böhringer, Judith |
|
dc.contributor.author |
Krägeloh-Mann, Ingeborg |
|
dc.contributor.author |
Schöls, Ludger |
|
dc.date.accessioned |
2020-01-28T14:56:05Z |
|
dc.date.available |
2020-01-28T14:56:05Z |
|
dc.date.issued |
2018 |
|
dc.identifier.issn |
1468-6244 |
|
dc.identifier.uri |
http://hdl.handle.net/10900/97474 |
|
dc.language.iso |
en |
de_DE |
dc.publisher |
Bmj Publishing Group |
de_DE |
dc.relation.uri |
http://dx.doi.org/10.1136/jmedgenet-2017-104622 |
de_DE |
dc.subject.ddc |
570 |
de_DE |
dc.subject.ddc |
610 |
de_DE |
dc.title |
SERAC1 deficiency causes complicated HSP: evidence from a novel splice mutation in a large family |
de_DE |
dc.type |
Article |
de_DE |
utue.quellen.id |
20190321153956_04673 |
|
utue.publikation.seiten |
39-47 |
de_DE |
utue.personen.roh |
Roeben, Benjamin |
|
utue.personen.roh |
Schuele, Rebecca |
|
utue.personen.roh |
Ruf, Susanne |
|
utue.personen.roh |
Bender, Benjamin |
|
utue.personen.roh |
Alhaddad, Bader |
|
utue.personen.roh |
Benkert, Tanja |
|
utue.personen.roh |
Meitinger, Thomas |
|
utue.personen.roh |
Reich, Selina |
|
utue.personen.roh |
Boehringer, Judith |
|
utue.personen.roh |
Langhans, Claus-Dieter |
|
utue.personen.roh |
Vaz, Frederic M. |
|
utue.personen.roh |
Wortmann, Saskia B. |
|
utue.personen.roh |
Marquardt, Thorsten |
|
utue.personen.roh |
Haack, Tobias B. |
|
utue.personen.roh |
Kraegeloh-Mann, Ingeborg |
|
utue.personen.roh |
Schoels, Ludger |
|
utue.personen.roh |
Synofzik, Matthis |
|
dcterms.isPartOf.ZSTitelID |
Journal of Medical Genetics |
de_DE |
dcterms.isPartOf.ZS-Issue |
1 |
de_DE |
dcterms.isPartOf.ZS-Volume |
55 |
de_DE |
utue.fakultaet |
04 Medizinische Fakultät |
de_DE |