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Article: NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect

TitleNDUFA9 point mutations cause a variable mitochondrial complex I assembly defect
Authors
Keywordsassembly
complex I
NDUFA9
OXPHOS
point mutation
Issue Date2018
Citation
Clinical Genetics, 2018, v. 93 n. 1, p. 111-118 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/248500
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorBaertling, F-
dc.contributor.authorSánche-Caballero, L-
dc.contributor.authorvan den Brand, MAM-
dc.contributor.authorFung, CW-
dc.contributor.authorChan, HSS-
dc.contributor.authorWong, CNV-
dc.contributor.authorHellebrekers, DME-
dc.contributor.authorde Coo, IFM-
dc.contributor.authorSmeitink, JAN AM-
dc.contributor.authorRodnburg, RJT-
dc.contributor.authorNijtmans, LGJ-
dc.date.accessioned2017-10-18T08:44:10Z-
dc.date.available2017-10-18T08:44:10Z-
dc.date.issued2018-
dc.identifier.citationClinical Genetics, 2018, v. 93 n. 1, p. 111-118-
dc.identifier.urihttp://hdl.handle.net/10722/248500-
dc.languageeng-
dc.relation.ispartofClinical Genetics-
dc.subjectassembly-
dc.subjectcomplex I-
dc.subjectNDUFA9-
dc.subjectOXPHOS-
dc.subjectpoint mutation-
dc.titleNDUFA9 point mutations cause a variable mitochondrial complex I assembly defect-
dc.typeArticle-
dc.identifier.emailChan, HSS: sophehs@hku.hk-
dc.identifier.emailWong, CNV: vcnwong@hku.hk-
dc.identifier.authorityChan, HSS=rp02210-
dc.identifier.authorityWong, CNV=rp00334-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1111/cge.13089-
dc.identifier.scopuseid_2-s2.0-85034750986-
dc.identifier.hkuros282128-
dc.identifier.volume93-
dc.identifier.issue1-
dc.identifier.spage111-
dc.identifier.epage118-
dc.identifier.isiWOS:000418355600012-

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