Outcomes of mitochondrial long chain fatty acid oxidation and carnitine defects from a single center metabolic genetics clinic.

Autor: Ambrose, Anastasia1 (AUTHOR), Sheehan, Melissa1 (AUTHOR), Bahl, Shalini2,3 (AUTHOR), Athey, Taryn1 (AUTHOR), Ghai-Jain, Shailly1 (AUTHOR), Chan, Alicia1 (AUTHOR), Mercimek-Andrews, Saadet1 (AUTHOR) saadet@ualberta.ca
Zdroj: Orphanet Journal of Rare Diseases. 9/15/2022, Vol. 17 Issue 1, p1-14. 14p.
Databáze: Academic Search Ultimate
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