Mapping of a locus for a familial autosomal recessive idiopathic myoclonic epilepsy of infancy to chromosome 16p13.

Myoclonic epilepsies with onset in infancy and childhood are clinically and etiologically heterogeneous. Although genetic factors are thought to play an important role, to date very little is known about the etiology of these disorders. We ascertained a large Italian pedigree segregating a recessive...

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Hlavní autoři: Zara, F, Gennaro, E, Stabile, M, Carbone, I, Malacarne, M, Majello, L, Santangelo, R, de Falco, F A, Bricarelli, F D
Médium: Artigo
Jazyk:Inglês
Vydáno: 2000
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1378007/
https://ncbi.nlm.nih.gov/pubmed/10741954
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