Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11

Reinson, Karit; Kovacs-Nagy, Reka; Oiglane-Shlik, Eve; Pajusalu, Sander; Noukas, Margit; Wintjes, Liesbeth T.; van den Brandt, Frans C. A.; Brink, Maaike; Acker, Till; Ahting, Uwe; Hahn, Andreas; Schanzer, Anne; Haack, Tobias B.; Rodenburg, Richard J.; Ounapa, Katrin

dc.contributor.author	Haack, Tobias
dc.date.accessioned	2020-07-27T10:41:10Z
dc.date.available	2020-07-27T10:41:10Z
dc.date.issued	2019
dc.identifier.issn	1878-0849
dc.identifier.uri	http://hdl.handle.net/10900/103894
dc.language.iso	en	de_DE
dc.publisher	Elsevier	de_DE
dc.relation.uri	http://dx.doi.org/10.1016/j.ejmg.2018.11.006	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11	de_DE
dc.type	Article	de_DE
utue.quellen.id	20200409032300_00765
utue.personen.roh	Reinson, Karit
utue.personen.roh	Kovacs-Nagy, Reka
utue.personen.roh	Oiglane-Shlik, Eve
utue.personen.roh	Pajusalu, Sander
utue.personen.roh	Noukas, Margit
utue.personen.roh	Wintjes, Liesbeth T.
utue.personen.roh	van den Brandt, Frans C. A.
utue.personen.roh	Brink, Maaike
utue.personen.roh	Acker, Till
utue.personen.roh	Ahting, Uwe
utue.personen.roh	Hahn, Andreas
utue.personen.roh	Schanzer, Anne
utue.personen.roh	Haack, Tobias B.
utue.personen.roh	Rodenburg, Richard J.
utue.personen.roh	Ounapa, Katrin
dcterms.isPartOf.ZSTitelID	European Journal of Medical Genetics	de_DE
dcterms.isPartOf.ZS-Issue	Article UNSP 103572	de_DE
dcterms.isPartOf.ZS-Volume	62	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE