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Peroxisomal 3‐ketoacyl‐CoA thiolase is partially processed in fibroblasts from patients with rhizomelic chondrodysplasia punctata
Author(s) -
Suzuki Y.,
Shimozawa N.,
Izai K.,
Uchida Y.,
Miura K.,
Akatsuka H.,
Nagaya M.,
Yamaguchi S.,
Orii T.
Publication year - 1993
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/bf00714280
Subject(s) - thiolase , medicine , peroxisomal disorder , pediatrics , medical school , peroxisome , medical education , receptor

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