d-3-Hydroxyacyl-CoA Dehydratase/d-3-Hydroxyacyl-CoA Dehydrogenase Bifunctional Protein Deficiency: A Newly Identified Peroxisomal Disorder

Author:

Suzuki Yasuyuki,Jiang Ling Ling,Souri Masayoshi,Miyazawa Shoko,Fukuda Seiji,Zhang Zhongyi,Une Mizuho,Shimozawa Nobuyuki,Kondo Naomi,Orii Tadao,Hashimoto Takashi

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference37 articles.

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3. Bile acid analyses in “pseudo-Zellweger” syndrome: clues to the defect in peroxisomal β-oxidation;Clayton;J Inherit Metab Dis,1988

4. Fukuda S, Suzuki Y, Shimozawa N, Zhang Z, Orii T, Aoyama T, Hashimoto T, et al. Amino acid and nucleotide sequences of human peroxisomal enoyl-CoA hydratase: 3-hydroxyacyl-CoA dehydrogenase cDNA. J Inherit Metab Dis (in press)

5. Properties of mitochondrial and peroxisomal enoyl-CoA hydratases from rat liver;Furuta;J Biochem (Tokyo),1980

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