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

Please use this identifier to cite or link to this item: http://repo.knmu.edu.ua/handle/123456789/7626

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DC Field	Value	Language
dc.contributor.author	Kvitchataya, Nataliya	-
dc.contributor.author	Grechanina, Juliya	-
dc.contributor.author	Yanovska, Anna	-
dc.date.accessioned	2014-11-17T08:51:16Z	-
dc.date.available	2014-11-17T08:51:16Z	-
dc.date.issued	2014	-
dc.identifier.citation	Kvitchataya 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.uri	https://repo.knmu.edu.ua/handle/123456789/7626	-
dc.description	observation 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.abstract	mitochondrial dysfunction manifestes with multiorganic disorders mainly affecting the central nervous system, heart, liver and muscles.	uk_UA
dc.language.iso	en	uk_UA
dc.subject	chromosomal abnormalities	uk_UA
dc.subject	mitochondrial dysfunction	uk_UA
dc.title	A child with combined chromosomal abnormalities, mitochondrial dysfunction and metabolic cobalamin disorder	uk_UA
dc.type	Thesis	uk_UA
Appears in Collections:	Наукові праці. Кафедра медичної генетики

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