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

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Title: Redefining the phenotype of alpha-methylacyl-CoA racemase (AMACR) deficiency.
Authors: 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)
Source: Orphanet Journal of Rare Diseases. 9/23/2024, Vol. 19 Issue 1, p1-9. 9p.
Database: Academic Search Ultimate
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  Data: Redefining the phenotype of alpha-methylacyl-CoA racemase (AMACR) deficiency.
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  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 9/23/2024, Vol. 19 Issue 1, p1-9. 9p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=179814085
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        Value: 10.1186/s13023-024-03358-9
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        Text: English
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      – TitleFull: Redefining the phenotype of alpha-methylacyl-CoA racemase (AMACR) deficiency.
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              Text: 9/23/2024
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              Y: 2024
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