Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families

Soehn, Anne S.; Rattay, Tim W.; Beck-Woedl, Stefanie; Schaeferhoff, Karin; Monk, David; Doebler-Neumann, Marion; Hoertnagel, Konstanze; Schluter, Agatha; Ruiz, Montserrat; Pujol, Aurora; Zuchner, Stephan; Riess, Olaf; Schule, Rebecca; Bauer, Peter; Schoels, Ludger

dc.contributor.author	Söhn, Anne
dc.contributor.author	Rattay, Tim Wilfried
dc.contributor.author	Beck-Wödl, Stefanie
dc.contributor.author	Schäferhoff, Karin
dc.contributor.author	Döbler-Neumann, Marion
dc.contributor.author	Rieß, Olaf
dc.contributor.author	Schüle-Freyer, Rebecca
dc.contributor.author	Bauer, Peter
dc.contributor.author	Schöls, Ludger
dc.date.accessioned	2019-03-01T13:21:37Z
dc.date.available	2019-03-01T13:21:37Z
dc.date.issued	2016
dc.identifier.issn	1526-632X
dc.identifier.uri	http://hdl.handle.net/10900/86580
dc.language.iso	en	de_DE
dc.publisher	Lippincott Williams & Wilkins	de_DE
dc.relation.uri	http://dx.doi.org/10.1212/WNL.0000000000002843	de_DE
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject.ddc	610	de_DE
dc.title	Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families	de_DE
dc.type	Article	de_DE
utue.quellen.id	20180405102126_02002
utue.publikation.seiten	186-191	de_DE
utue.personen.roh	Soehn, Anne S.
utue.personen.roh	Rattay, Tim W.
utue.personen.roh	Beck-Woedl, Stefanie
utue.personen.roh	Schaeferhoff, Karin
utue.personen.roh	Monk, David
utue.personen.roh	Doebler-Neumann, Marion
utue.personen.roh	Hoertnagel, Konstanze
utue.personen.roh	Schluter, Agatha
utue.personen.roh	Ruiz, Montserrat
utue.personen.roh	Pujol, Aurora
utue.personen.roh	Zuchner, Stephan
utue.personen.roh	Riess, Olaf
utue.personen.roh	Schule, Rebecca
utue.personen.roh	Bauer, Peter
utue.personen.roh	Schoels, Ludger
dcterms.isPartOf.ZSTitelID	Neurology	de_DE
dcterms.isPartOf.ZS-Issue	2	de_DE
dcterms.isPartOf.ZS-Volume	87	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE