Pontocerebellar hypoplasia type 11: Does the genetic defect determine timing of cerebellar pathology?

Laugwitz, Lucia; Buchert, Rebecca; Groeschel, Samuel; Riess, Angelika; Grimmel, Mona; Beck-Woedl, Stefanie; Sturm, Marc; Gohla, Georg; Doebler-Neumann, Marion; Kraegeloh-Mann, Ingeborg; Haack, Tobias B.

dc.contributor.author	Laugwitz, Lucia
dc.contributor.author	Buchert, Rebecca
dc.contributor.author	Grimmel, Mona
dc.contributor.author	Sturm, Marc
dc.contributor.author	Gohla, Georg
dc.contributor.author	Gröschel, Samuel
dc.contributor.author	Riess, Angelika
dc.contributor.author	Beck-Wödl, Stefanie
dc.contributor.author	Döbler-Neumann, Marion
dc.contributor.author	Krägeloh-Mann, Ingeborg
dc.contributor.author	Haack, Tobias
dc.date.accessioned	2021-06-22T08:00:27Z
dc.date.available	2021-06-22T08:00:27Z
dc.date.issued	2020
dc.identifier.issn	1878-0849
dc.identifier.uri	http://hdl.handle.net/10900/116388
dc.language.iso	en	de_DE
dc.publisher	Elsevier	de_DE
dc.relation.uri	http://dx.doi.org/10.1016/j.ejmg.2020.103938	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Pontocerebellar hypoplasia type 11: Does the genetic defect determine timing of cerebellar pathology?	de_DE
dc.type	Article	de_DE
utue.quellen.id	20210304112512_01808
utue.personen.roh	Laugwitz, Lucia
utue.personen.roh	Buchert, Rebecca
utue.personen.roh	Groeschel, Samuel
utue.personen.roh	Riess, Angelika
utue.personen.roh	Grimmel, Mona
utue.personen.roh	Beck-Woedl, Stefanie
utue.personen.roh	Sturm, Marc
utue.personen.roh	Gohla, Georg
utue.personen.roh	Doebler-Neumann, Marion
utue.personen.roh	Kraegeloh-Mann, Ingeborg
utue.personen.roh	Haack, Tobias B.
dcterms.isPartOf.ZSTitelID	European Journal of Medical Genetics	de_DE
dcterms.isPartOf.ZS-Issue	Article 103938	de_DE
dcterms.isPartOf.ZS-Volume	63 (7)	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE