Zobrazeno 1 - 2
of 2
pro vyhledávání: '"L. N. Taran"'
Autor:
A. I. Pazniak, A. A. Tolkachikova, N. N. Gundilovich, Yu. A. Klimosh, S. E. Barantseva, L. N. Taran
Publikováno v:
Proceedings of the National Academy of Sciences of Belarus, Chemical Series. 56:114-124
The paper presents the study results of diabases of rare-earth and beryllium-containing deposit of the Republicof Belarusin order to determine their suitability for the production of silicate materials and products for various purposes. The data obta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b7e34103d73a27197f328081bde2646
https://doi.org/10.29235/1561-8331-2020-56-1-114-124
https://doi.org/10.29235/1561-8331-2020-56-1-114-124
Autor:
A. A. Lebedenko, S. B. Berezhanskay, A. S. Todorova, N. N. Vostrykh, E. Y. Kaushanskay, E. A. Lukyanova, E. A. Papsheva, G. N. Smykova, L. N. Taranenko
Publikováno v:
Медицинский вестник Юга России, Vol 11, Iss 4, Pp 84-91 (2020)
Glutaric aciduria type I (deficiency of glutaryl-COA dehydrogenase, glutaric acidemia type I) is a rare autosomal recessive disease caused by mutations in the gene encoding the enzyme glutaryl – COA - dehydrogenase (GCDH). Cerebral organic aciduria
Externí odkaz:
https://doaj.org/article/d23abdde30684fdb8b0aa36489a8fa50