Partial epilepsy in a girl with a symptom-free sister: first two Finnish patients with dihydropyrimidine dehydrogenase deficiency




Holopainen I, Pulkki K, Heinonen OJ, Näntö-Salonen K, Haataja L, Greter J, Holme E, van Kuilenburg AB, Vreken P, van Gennip AH

1997

Journal of Inherited Metabolic Disease

Journal of inherited metabolic disease

J Inherit Metab Dis

20

5

719

20

2

0141-8955

DOIhttps://doi.org/10.1023/A:1005399131620




Last updated on 2024-26-11 at 20:09