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
DOI: https://doi.org/10.1023/A:1005399131620