Facioscapulohumeral muscular dystrophy: genetics, gene activation and downstream signalling with regard to recent therapeutic approaches: an update

dc.contributor.author	Deigner, Hans-Peter
dc.date.accessioned	2021-08-31T06:32:04Z
dc.date.available	2021-08-31T06:32:04Z
dc.date.issued	2021
dc.identifier.issn	1750-1172
dc.identifier.uri	http://hdl.handle.net/10900/118358
dc.language.iso	en	de_DE
dc.publisher	Bmc	de_DE
dc.relation.uri	http://dx.doi.org/10.1186/s13023-021-01760-1	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Facioscapulohumeral muscular dystrophy: genetics, gene activation and downstream signalling with regard to recent therapeutic approaches: an update	de_DE
dc.type	Article	de_DE
utue.quellen.id	20210512015105_00412
utue.personen.roh	Schaetzl, Teresa
utue.personen.roh	Kaiser, Lars
utue.personen.roh	Deigner, Hans-Peter
dcterms.isPartOf.ZSTitelID	Orphanet Journal of Rare Diseases	de_DE
dcterms.isPartOf.ZS-Issue	Article 129	de_DE
dcterms.isPartOf.ZS-Volume	16	de_DE
utue.fakultaet	07 Mathematisch-Naturwissenschaftliche Fakultät	de_DE