A child with combined chromosomal abnormalities, mitochondrial dysfunction and metabolic cobalamin disorder

dc.contributor.authorKvitchataya, Nataliya
dc.contributor.authorGrechanina, Juliya
dc.contributor.authorYanovska, Anna
dc.date.accessioned2014-11-17T08:51:16Z
dc.date.available2014-11-17T08:51:16Z
dc.date.issued2014
dc.descriptionobservation demonstrates the combination of chromosome pathology with metabolic disorders, it is necessary to investigate chromosomal aberrations of metabolic status for the selection of adequate therapy.uk_UA
dc.description.abstractmitochondrial dysfunction manifestes with multiorganic disorders mainly affecting the central nervous system, heart, liver and muscles.uk_UA
dc.identifier.citationKvitchataya N. N. A child with combined chromosomal abnormalities, mitochondrial dysfunction and metabolic cobalamin disorder / N. N. Kvitchataya, Y. B. Grechanina, A. A. Yanovska // Journal of Inherited Metabolic Disease. — 2014. — Vol. 37, suppl. 1 : Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Innsbruck, 2–5 September, 2014 : abstracts. — P. 184.uk_UA
dc.identifier.urihttps://repo.knmu.edu.ua/handle/123456789/7626
dc.language.isoenuk_UA
dc.subjectchromosomal abnormalitiesuk_UA
dc.subjectmitochondrial dysfunctionuk_UA
dc.titleA child with combined chromosomal abnormalities, mitochondrial dysfunction and metabolic cobalamin disorderuk_UA
dc.typeThesisuk_UA

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