Dihydropyridmidinase deficiency and congenital microvillous atrophy: Coincidence or genetic relation?
Author:
Affiliation:
1. ; University Children's Hospital; Marburg Germany
2. ; University Children's Hospital; Utrecht The Netherlands
3. ; University Children's Hospital; Amsterdam The Netherlands
4. ; University Children's Hospital; Nijmegen The Netherlands
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005374426168/fullpdf
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3. Bindl L Kirschstein M Keller K Lentze MJ Phillips AD 1996 Characteristic tubular proteinuria in congenital microvillous atrophy ESPGAN 6/1996
4. Phytosterolemia in children with parenteral nutrition-associated liver disease;Clayton;Gastroenterology,1993
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