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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Zara, F, Gennaro, E, Stabile, M, Carbone, I, Malacarne, M, Majello, L, Santangelo, R, de Falco, F A, Bricarelli, F D
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2000
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC1378007/
https://ncbi.nlm.nih.gov/pubmed/10741954
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