A duplication in 1q21.3 in a family with early onset and childhood absence epilepsy.

Muhle, Hiltrud

A duplication in 1q21.3 in a family with early onset and childhood absence epilepsy. [electronic resource] - Epilepsia Dec 2010 - 2453-6 p. digital

Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't

1528-1167

10.1111/j.1528-1167.2010.02712.x doi


Adenosine Deaminase--genetics
Adolescent
Chromosomes, Human, Pair 1--genetics
Epilepsy, Absence--diagnosis
Epilepsy, Generalized--genetics
Family
Female
Gene Duplication--genetics
Humans
Male
Pedigree
RNA-Binding Proteins
Receptors, Nicotinic--genetics