Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency

Brage Storstein Andresen(Aarhus University), S. E. Olpin(Sheffield Children's Hospital), Ben J. H. M. Poorthuis(Leiden University Medical Center), H.R. Scholte(Erasmus University Rotterdam), Christine Vianey‐Saban(Hôpital Debrousse), Ronald Wanders(University of Amsterdam), Lodewijk IJlst(University of Amsterdam), Andrew A.M. Morris(Royal Victoria Infirmary), Morteza Pourfarzam(Royal Victoria Infirmary), K. Bartlett(Royal Victoria Infirmary), E. R. Baumgartner(University Children’s Hospital Basel), Johannis B.C. deKlerk(Hôpital Debrousse), Lisbeth Dahl Schroeder(Aarhus University), Thomas J. Corydon(Aarhus University), Hans Lund(Aarhus University Hospital), Vibeke Winter(Aarhus University Hospital), Peter Bross(Aarhus University Hospital), Lars Bolund(Aarhus University), Niels Gregersen(Aarhus University Hospital)
The American Journal of Human Genetics
February 1, 1999
Cited by 301Open Access
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