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Article: Human d-lactate dehydrogenase deficiency by LDHD mutation in a patient with neurological manifestations and mitochondrial complex IV deficiency

TitleHuman d-lactate dehydrogenase deficiency by LDHD mutation in a patient with neurological manifestations and mitochondrial complex IV deficiency
Authors
Kwong, KYWong, SSNRodenburg, RJTSmeitink, JChan, GCFFung, CW
Issue Date2021
Citation
JIMD Report, 2021, v. 60 n. 1, p. 15-22 How to Cite?
DOI: http://dx.doi.org/10.1002/jmd2.12220
Persistent Identifierhttp://hdl.handle.net/10722/319281

 

DC FieldValueLanguage
dc.contributor.authorKwong, KY-
dc.contributor.authorWong, SSN-
dc.contributor.authorRodenburg, RJT-
dc.contributor.authorSmeitink, J-
dc.contributor.authorChan, GCF-
dc.contributor.authorFung, CW-
dc.date.accessioned2022-10-14T05:10:27Z-
dc.date.available2022-10-14T05:10:27Z-
dc.date.issued2021-
dc.identifier.citationJIMD Report, 2021, v. 60 n. 1, p. 15-22-
dc.identifier.urihttp://hdl.handle.net/10722/319281-
dc.languageeng-
dc.relation.ispartofJIMD Report-
dc.titleHuman d-lactate dehydrogenase deficiency by LDHD mutation in a patient with neurological manifestations and mitochondrial complex IV deficiency-
dc.typeArticle-
dc.identifier.emailKwong, KY: kkyanna@hku.hk-
dc.identifier.emailChan, GCF: gcfchan@hku.hk-
dc.identifier.authorityChan, GCF=rp00431-
dc.identifier.doi10.1002/jmd2.12220-
dc.identifier.hkuros339348-
dc.identifier.volume60-
dc.identifier.issue1-
dc.identifier.spage15-
dc.identifier.epage22-

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