Literature DB >> 2737377

Peroxisomopathies: new developments.

H Zellweger.   

Abstract

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Year:  1989        PMID： 2737377     DOI： 10.1111/j.1469-8749.1989.tb03989.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN： 0012-1622            Impact factor:   5.449


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  3 in total

1.  Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme.

Authors:  J C Heikoop; C W van Roermund; W W Just; R Ofman; R B Schutgens; H S Heymans; R J Wanders; J M Tager
Journal:  J Clin Invest       Date:  1990-07       Impact factor: 14.808

2.  Autopsy findings in two siblings with infantile Refsum disease.

Authors:  C W Chow; A Poulos; A J Fellenberg; J Christodoulou; D M Danks
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

3.  Differential protein import deficiencies in human peroxisome assembly disorders.

Authors:  A Motley; E Hettema; B Distel; H Tabak
Journal:  J Cell Biol       Date:  1994-05       Impact factor: 10.539
  3 in total

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