Deficient activities and proteins of peroxisomal β-oxidation enzymes in infants with Zellweger syndrome-Reference-Cited by-同舟云学术

Deficient activities and proteins of peroxisomal β-oxidation enzymes in infants with Zellweger syndrome

Published:1986-04 Issue:2 Volume:156 Page:191-196
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Suzuki Yasuyuki,Orii Tadao,Mori Masataka,Tatibana Masamiti,Hashimoto Takashi

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference23 articles.

1. A familial syndrome of multiple congenital defects;Bowen;Bull Johns Hopkins Hosp,1964

2. Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acids;Brown;Johns Hopkins Med J,1982

3. Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome);Heymans;Nature (London),1983

4. Defects of bile acid synthesis in Zellweger's syndrome;Hanson;Science,1979

5. Cerebro-hepato-renal syndrome of Zellweger;Danks;J Pediatr,1975

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