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CoA-dependent activation of mitochondrial acyl carrier protein links four neurodegenerative diseases
Autor:
Lambrechts, R. A. (Roald A.), Schepers, H. (Hein), Yu, Y. (Yi), van der Zwaag, M. (Marianne), Autio, K. J. (Kaija J.), Vieira‐Lara, M. A. (Marcel A.), Bakker, B. M. (Barbara M.), Tijssen, M. A. (Marina A.), Hayflick, S. J. (Susan J.), Grzeschik, N. A. (Nicola A.), Sibon, O. C. (Ody C. M.)
PKAN, CoPAN, MePAN, and PDH‐E2 deficiency share key phenotypic features but harbor defects in distinct metabolic processes. Selective damage to the globus pallidus occurs in these genetic neurodegenerative diseases, which arise from defects in CoA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2423::d2eea56474e960514b3f1f5f50a06c81
http://urn.fi/urn:nbn:fi-fe2020040110004
http://urn.fi/urn:nbn:fi-fe2020040110004
