Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Movement Disorders/enzymology"'
Autor:
Braissant, O., Henry, H.
Publikováno v:
Journal of Inherited Metabolic Disease, vol. 31, no. 2, pp. 230-239
Creatine deficiency syndromes, either due to AGAT, GAMT or SLC6A8 deficiencies, lead to a complete absence, or a very strong decrease, of creatine within the brain, as measured by magnetic resonance spectroscopy. While the mammalian central nervous s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1900::f911dfd182fb8b72e3f3786f5a236cda
https://serval.unil.ch/notice/serval:BIB_F13D66EBFC62
https://serval.unil.ch/notice/serval:BIB_F13D66EBFC62
