Redefining the phenotype of alpha-methylacyl-CoA racemase (AMACR) deficiency.

Autor: Klouwer, Femke C.C.1 (AUTHOR) f.c.klouwer@amsterdamumc.nl, Roosendaal, Stefan D.2 (AUTHOR), Hollak, Carla E. M.3 (AUTHOR), Langeveld, Mirjam3 (AUTHOR), Poll-The, Bwee Tien1 (AUTHOR), Sorge, Arlette J. van4 (AUTHOR), Wolf, Nicole I.1,5 (AUTHOR), Knaap, Marjo S. van der1,5 (AUTHOR), Engelen, Marc1 (AUTHOR)
Zdroj: Orphanet Journal of Rare Diseases. 9/23/2024, Vol. 19 Issue 1, p1-9. 9p.
Databáze: Academic Search Ultimate
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