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Dihydropyridmidinase deficiency and congenital microvillous atrophy: Coincidence or genetic relation?

✍ Scribed by B. Assmann; G. F. Hoffmann; L. Wagner; C. Bräutigam; H. W. Seyberth; M. Duran; A. B. P. Van Kuilenburg; R. Wevers; A. H. Van Gennip


Book ID
110224201
Publisher
Springer
Year
1997
Tongue
English
Weight
46 KB
Volume
20
Category
Article
ISSN
0141-8955

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