Development of Molecular Identification Method for GenusAlexandrium(Dinophyceae) Using Whole-Cell FISH

Identification of the molecular defect i

Identification of the molecular defect in patients with peroxisomal mosaicism using a novel method involving culturing of cells at 40°C: Implications for other inborn errors of metabolism

✍ Jeannette Gootjes; Frank Schmohl; Petra A.W. Mooijer; Conny Dekker; Hanna Mandel 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 428 KB

## Communicated by Johannes Zschocke The peroxisome biogenesis disorders (PBDs), which comprise Zellweger syndrome (ZS), neonatal adrenoleukodystrophy, and infantile Refsum disease (IRD), represent a spectrum of disease severity, with ZS being the most severe, and IRD the least severe disorder. Th