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Partial epilepsy in a girl with a symptom‐free sister: First two Finnish patients with dihydropyrimidine dehydrogenase deficiency
Author(s) -
Holopainen I.,
Pulkki K.,
Hein O.J.,
NäntöSalonen K.,
Haataja L.,
Greter J.,
Holme E.,
Kuilenburg A.B.P.,
Vreken P.,
Gennip A.H.
Publication year - 1997
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1023/a:1005399131620
Subject(s) - medicine , university hospital , pediatrics , pediatric neurology , family medicine