Recommendations for patient screening in ultra-rare inherited metabolic diseases : what have we learned from Niemann-Pick disease type C?

Sobrido, Maria-Jesus; Bauer, Peter; de Koning, Tom; Klopstock, Thomas; Nadjar, Yann; Patterson, Marc C.; Synofzik, Matthis; Hendriksz, Chris J.

dc.contributor.author	Bauer, Peter
dc.contributor.author	Synofzik, Matthis
dc.date.accessioned	2020-06-16T07:05:11Z
dc.date.available	2020-06-16T07:05:11Z
dc.date.issued	2019
dc.identifier.issn	1750-1172
dc.identifier.uri	http://hdl.handle.net/10900/101490
dc.language.iso	en	de_DE
dc.publisher	Bmc	de_DE
dc.relation.uri	http://dx.doi.org/10.1186/s13023-018-0985-1	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Recommendations for patient screening in ultra-rare inherited metabolic diseases : what have we learned from Niemann-Pick disease type C?	de_DE
dc.type	Article	de_DE
utue.quellen.id	20190926111821_02971
utue.personen.roh	Sobrido, Maria-Jesus
utue.personen.roh	Bauer, Peter
utue.personen.roh	de Koning, Tom
utue.personen.roh	Klopstock, Thomas
utue.personen.roh	Nadjar, Yann
utue.personen.roh	Patterson, Marc C.
utue.personen.roh	Synofzik, Matthis
utue.personen.roh	Hendriksz, Chris J.
dcterms.isPartOf.ZSTitelID	Orphanet Journal of Rare Diseases	de_DE
dcterms.isPartOf.ZS-Issue	Article 20	de_DE
dcterms.isPartOf.ZS-Volume	14	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE