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Dihydropyridmidinase deficiency and congenital microvillous..:
Assmann, B.
;
Hoffmann, G. F.
;
Wagner, L.
...
Journal of Inherited Metabolic Disease. 20 (1997) 5 - p. 681-688 , 1997
Link:
https://doi.org/10.1023/a:1005374426168
RT Journal T1 <Title>Dihydropyridmidinase deficiency and congenital microvillous atrophy: Coincidence or genetic relation?</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1023_a:1005374426168&Exemplar=1&LAN=DE A1 Assmann, B. A1 Hoffmann, G. F. A1 Wagner, L. A1 Bräutigam, C. A1 Seyberth, H. W. A1 Duran, M. A1 Van Kuilenburg, A. B. P. A1 Wevers, R. A1 Van Gennip, A. H. PB Wiley YR 1997 SN 0141-8955 SN 1573-2665 JF Journal of Inherited Metabolic Disease VO 20 IS 5 SP 681 OP 688 LK http://dx.doi.org/https://doi.org/10.1023/a:1005374426168 DO https://doi.org/10.1023/a:1005374426168 SF ELIB - SuUB Bremen
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