Please use this identifier to cite or link to this item: http://repo.knmu.edu.ua/handle/123456789/18953
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dc.contributor.authorGrechanina, Elena-
dc.contributor.authorGrechanina, Juliya-
dc.contributor.authorBiletska, Svetlana-
dc.contributor.authorMaksutina, Irina-
dc.date.accessioned2017-12-15T12:38:08Z-
dc.date.available2017-12-15T12:38:08Z-
dc.date.issued2017-04-25-
dc.identifier.citationA rare disease of the mitochondrial respiratory chain – 3-methylglutaconic aciduria. Approach to diagnosis and rehabilitation / O. Grechanina, Y. Grechanina, S. Biletska, I. Maksyutina // Сборникът се издава от Българска Асоциация за Промоция на Образование и Наука (БАПОН). – 2017. – № 2. – C. 30.ru_RU
dc.identifier.urihttp://repo.knmu.edu.ua/handle/123456789/18953-
dc.description.abstractTo study the clinical phenotype of a rare disease, to evaluate the effect of synthropy on the clinical and biochemical features of the pathology for developing a strategy for improving the quality of life of patients.ru_RU
dc.language.isoenru_RU
dc.subject3-methylglutaconic aciduriaru_RU
dc.subject3-methylglutaconic aciduriaru_RU
dc.titleA rare disease of the mitochondrial respiratory chain – 3-methylglutaconic aciduria. Approach to diagnosis and rehabilitationru_RU
dc.typeArticleru_RU
Appears in Collections:Наукові праці. Кафедра медичної генетики

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