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المؤلفون: E. Faleschini, B. Bortot, Giovanni Maria Severini, Stefania Biffi, Corrado Angelini, Egidio Barbi, Marco Carrozzi
المساهمون: Bortot, B., Barbi, E., Biffi, S., Angelini, C., Faleschini, E., Severini, G. M., Carrozzi, M.
مصطلحات موضوعية: Respiratory chain, Child, Polyendocrinopathies, Autoimmune, medicine.diagnostic_test, Lactic, Muscles, Autoimmune polyendocrinopathy, Mitochondrial, Mitochondria, Lactic acidosis, Met, Muscle, Molecular Medicine, Acidosis, Lactic, Female, medicine.symptom, Acidosis, Human, medicine.medical_specialty, Mitochondrial DNA, RNA, Transfer, Met, Exercise intolerance, Biology, DNA, Mitochondrial, Mitochondrial Proteins, Internal medicine, medicine, Humans, Mitochondrial Protein, Point Mutation, Met-tRNA and Cox III cosegregating mutations, Prostaglandin-Endoperoxide Synthases, Molecular Biology, Cell Biology, Autoimmune disease, Muscle biopsy, Point mutation, Met-tRNA and Cox III cosegregating mutation, Prostaglandin-Endoperoxide Synthase, DNA, medicine.disease, Transfer, Endocrinology, Polyendocrinopathies, RNA, Autoimmune
وصف الملف: STAMPA
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3765aa0a15c2c2deb8aa3d7d7ebeb47b
https://hdl.handle.net/11368/2920436 -
2دورية أكاديمية
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