A rare disease of the mitochondrial respiratory chain – 3-methylglutaconic aciduria. Approach to diagnosis and rehabilitation

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.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.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.urihttps://repo.knmu.edu.ua/handle/123456789/18953
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

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