The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8.

A recently delineated childhood epilepsy has hitherto been observed only in a small geographic region in northern Finland, where, with the exception of one, both parents of all of the 11 sibships with affected individuals descend from one or two founding couples. The disease is characterized by gene...

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Bibliografiska uppgifter
Huvudupphovsmän: Tahvanainen, E, Ranta, S, Hirvasniemi, A, Karila, E, Leisti, J, Sistonen, P, Weissenbach, J, Lehesjoki, A E, de la Chapelle, A
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1994
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC44380/
https://ncbi.nlm.nih.gov/pubmed/8041778
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