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See Latest ArticlesFamilial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance
Human Molecular Genetics, 09/15/09
Dibbens LM et al. – The odds ratio is 68 (95% confidence interval 29–181), indicating a pathogenic lesion predisposing to epilepsy with complex inheritance and incomplete penetrance for the IGE component of the phenotype in multiplex families.
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A family with autosomal dominant leukodystrophy linked to 5q23.2–q23.3 without lamin B1 mutations
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