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pro vyhledávání: '"Alexander V. Kuzin"'
Autor:
S. Makarov, Khalid G. Ismailov, Elena A. Dolzhenkova, Elena M. Zaytseva, Natalia N. Politova, V N Amirdzhanova, Vadim V. Zar, Jahangir S. Agzamov, Alexander V. Kuzin
Publikováno v:
Medical and Social Expert Evaluation and Rehabilitation. 23:42-45
Background. Alkaptonuria is an orphan, autosomal recessive disease in which clinical symptoms debut in adulthood and are characterized by progressive degenerative changes in large joints (knee, hip, shoulder) and the spine, often leading to the need
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5be7cb2080ad424d42fd74002354f68a
https://doi.org/10.17816/mser35167
https://doi.org/10.17816/mser35167
