A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of Acyl-CoA oxidase (pseudo–Neonatal adrenoleukodystrophy)

In the present paper two siblings are presented with clinical manifestations very similar to those of patients affected by neonatal adrenoleukodystrophy. In contrast to neonatal adrenoleukodystrophy patients, hepatic peroxisomes in these siblings were enlarged in size and not decreased in number. Ac...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Hoofdauteurs: Poll-The, Bwee Tien, Roels, Frank, Ogier, Hélène, Scotto, Jacques, Vamecq, Joseph, Schutgens, Ruud B. H., Wanders, Ronald J. A., van Roermund, Carlo W. T., van Wijland, Michil J. A., Schram, Adre W., Tager, Joseph M., Saudubray, Jean-Marie
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1988
Onderwerpen:
Original Articles
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715143/
https://ncbi.nlm.nih.gov/pubmed/2894756
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!

Gelijkaardige items