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PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.

The peroxisome-biogenesis disorders (PBDs) are a genetically and phenotypically diverse group of diseases caused by defects in peroxisome assembly. One of the milder clinical variants within the PBDs is neonatal adrenoleukodystrophy (NALD), a disease that is usually associated with partial defects i...

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Bibliografische gegevens
Hoofdauteurs: Liu, Y, Björkman, J, Urquhart, A, Wanders, R J, Crane, D I, Gould, S J
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1999
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377968/
https://ncbi.nlm.nih.gov/pubmed/10441568
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