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Reinvestigation of peroxisomal 3-ketoacyl-CoA thiolase deficiency: identification of the true defect at the level of d-bifunctional protein. [electronic resource] by
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- Denis, S
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- Goldfischer, S
- Wanders, R J A
Producer: 20020627
In:
American journal of human genetics vol. 70
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Mitochondrial acetoacetyl-CoA thiolase deficiency: basal ganglia impairment may occur independently of ketoacidosis. [electronic resource] by
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- Benoist, Jean-François
- de Lonlay, Pascale
- Dobbelaere, Dries
- Fouilhoux, Alain
- Guffon, Nathalie
- Rouvet, Isabelle
- Labarthe, François
- Mention, Karine
- Touati, Guy
- Valayannopoulos, Vassili
- Ogier de Baulny, Hélène
- Elmaleh-Bergès, Monique
- Acquaviva-Bourdain, Cécile
- Vianey-Saban, Christine
- Schiff, Manuel
Producer: 20170824
In:
Journal of inherited metabolic disease vol. 40
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ACAT inhibition reduces the progression of preexisting, advanced atherosclerotic mouse lesions without plaque or systemic toxicity. [electronic resource] by
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- Mayne, Jeffrey
- Kusunoki, Jun
- Miller, Christine
- Davis, Matthew
- Wilson, Martha
- Dehn, Shirley
- Thorp, Edward
- Tabas, Ira
- Taubman, Mark B
- Rudel, Lawrence L
- Fisher, Edward A
Producer: 20130212
In:
Arteriosclerosis, thrombosis, and vascular biology vol. 33
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Identification of a novel missense mutation of PEX7 gene in an Iranian patient with rhizomelic chondrodysplasia punctata type 1. [electronic resource] by
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- Salamian, Ahmad
- Tanhaie, Somayeh
- Karamali, Fereshteh
- Rabiee, Farzaneh
- Parivar, Kazem
- Baharvand, Hossein
- Nasr-Esfahani, Mohammad Hossein
Producer: 20130430
In:
Gene vol. 518
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Functional TLR5 genetic variants affect human colorectal cancer survival. [electronic resource] by
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- Försti, Asta
- Eckert, Jana
- Knezevic, Jelena
- Bevier, Melanie
- von Schönfels, Witigo
- Heits, Nils
- Walter, Jessica
- Hinz, Sebastian
- Lascorz, Jesus
- Hampe, Jochen
- Hartl, Dominik
- Frick, Julia-Stefanie
- Hemminki, Kari
- Schafmayer, Clemens
- Weber, Alexander N R
Producer: 20140513
In:
Cancer research vol. 73
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