The segregation of glutaryl-CoA dehydrogenase deficiency and Refsum syndrome in a family
E. Christensen
Section of Clinical Genetics, University Department of Paediatrics, Rigshospitalet, Copenhagen, Denmark
Search for more papers by this authorN. J. Brandt
Section of Clinical Genetics, University Department of Paediatrics, Rigshospitalet, Copenhagen, Denmark
Search for more papers by this authorT. Rosenberg
National Eye Clinic for the Visually Impaired, Hellerup, Denmark
Search for more papers by this authorK. Bömers
Neurological Department, Esbjerg Centralsygehus, Esbjerg, Denmark
Search for more papers by this authorC. Jakobs
Department of Paediatrics, Free University Hospital, Amsterdam, The Netherlands
Search for more papers by this authorE. Christensen
Section of Clinical Genetics, University Department of Paediatrics, Rigshospitalet, Copenhagen, Denmark
Search for more papers by this authorN. J. Brandt
Section of Clinical Genetics, University Department of Paediatrics, Rigshospitalet, Copenhagen, Denmark
Search for more papers by this authorT. Rosenberg
National Eye Clinic for the Visually Impaired, Hellerup, Denmark
Search for more papers by this authorK. Bömers
Neurological Department, Esbjerg Centralsygehus, Esbjerg, Denmark
Search for more papers by this authorC. Jakobs
Department of Paediatrics, Free University Hospital, Amsterdam, The Netherlands
Search for more papers by this author
References
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