Title: |
A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 °C |
Source: |
Journal of Human Genetics
[1434-5161]
Zeharia,
Avraham
yr:2007
|
|
|
|