A novelPEX12mutation 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
Avraham Zeharia, Merel S. Ebberink, Ronald J. A. Wanders, Hans R. Waterham, Alisa Gutman, Andreea Nissenkorn, Stanley H. KormanVolume:
52
Language:
english
Pages:
8
DOI:
10.1007/s10038-007-0157-y
Date:
July, 2007
File:
PDF, 212 KB
english, 2007