Peroxisomal assembly defects: Clinical, pathologic, and biochemical findings in two patients in a newly identified complementation group-Reference-Cited by-同舟云学术

Peroxisomal assembly defects: Clinical, pathologic, and biochemical findings in two patients in a newly identified complementation group

Published:1995-10 Issue:4 Volume:127 Page:596-599
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Poulos Alfred,Christodoulou John,Chow Chung W.,Goldblatt Jack,Paton Barbara C.,Orii Tadao,Suzuki Yasuyuki,Shimozawa Nobuyuki

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference13 articles.

1. Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome;Goldfischer;Science,1973

2. Morphometry of peroxisomes and immunolocalization of peroxisomal proteins in the liver of patients with generalized peroxisomal disorders;Hughes;Virchows Archiv A Pathol Anat Histopathol,1993

3. Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect;Shimozawa;Am J Hum Genet,1993

4. Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells;Yajima;Hum Genet,1992

5. Accumulation of pristanic acid (2,6,10,14 tetramethylpentadecanoic acid) in the plasma of patients with generalized peroxisomal dysfunction;Poulos;Eur J Pediatr,1988

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