Disorders of peroxisome biogenesis: Complementation analysis shows geneticheterogeneity with strong overrepresentation of one group (PEX1 deficiency)

Authors
Wanders, RJA Mooijer, PAW Dekker, C Suzuki, Y Shimozawa, N
Citation
Rja. Wanders et al., Disorders of peroxisome biogenesis: Complementation analysis shows geneticheterogeneity with strong overrepresentation of one group (PEX1 deficiency), J INH MET D, 22(3), 1999, pp. 314-318
Citations number
17
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
JOURNAL OF INHERITED METABOLIC DISEASE
ISSN journal
01418955 → ACNP
Volume
22
Issue
3
Year of publication
1999
Pages
314 - 318
Database
ISI
SICI code
0141-8955(199905)22:3<314:DOPBCA>2.0.ZU;2-D