MAPT p.V363I mutation A rare cause of corticobasal degeneration

Ahmed, Sarah; Fairen, Monica Diez; Sabir, Marya S.; Pastor, Pau; Ding, Jinhui; Ispierto, Lourdes; Butala, Ankur; Morris, Christopher M.; Schulte, Claudia; Gasser, Thomas; Jabbari, Edwin; Pletnikova, Olga; Morris, Huw R.; Troncoso, Juan; Gelpi, Ellen; Pantelyat, Alexander; Scholz, Sonja W.

dc.contributor.author	Schulte, Claudia
dc.contributor.author	Gasser, Thomas
dc.date.accessioned	2020-03-16T08:10:18Z
dc.date.available	2020-03-16T08:10:18Z
dc.date.issued	2019
dc.identifier.issn	2376-7839
dc.identifier.uri	http://hdl.handle.net/10900/99068
dc.language.iso	en	de_DE
dc.publisher	Lippincott Williams & Wilkins	de_DE
dc.relation.uri	http://dx.doi.org/10.1212/NXG.0000000000000347	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	MAPT p.V363I mutation A rare cause of corticobasal degeneration	de_DE
dc.type	Article	de_DE
utue.quellen.id	20190926111821_00290
utue.personen.roh	Ahmed, Sarah
utue.personen.roh	Fairen, Monica Diez
utue.personen.roh	Sabir, Marya S.
utue.personen.roh	Pastor, Pau
utue.personen.roh	Ding, Jinhui
utue.personen.roh	Ispierto, Lourdes
utue.personen.roh	Butala, Ankur
utue.personen.roh	Morris, Christopher M.
utue.personen.roh	Schulte, Claudia
utue.personen.roh	Gasser, Thomas
utue.personen.roh	Jabbari, Edwin
utue.personen.roh	Pletnikova, Olga
utue.personen.roh	Morris, Huw R.
utue.personen.roh	Troncoso, Juan
utue.personen.roh	Gelpi, Ellen
utue.personen.roh	Pantelyat, Alexander
utue.personen.roh	Scholz, Sonja W.
dcterms.isPartOf.ZSTitelID	Neurology - Genetics	de_DE
dcterms.isPartOf.ZS-Issue	Article UNSP e347	de_DE
dcterms.isPartOf.ZS-Volume	5	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE