Benign familial neonatal convulsions: evidence for clinical and genetic heterogeneity.

Ryan, S G

Benign familial neonatal convulsions: evidence for clinical and genetic heterogeneity. [electronic resource] - Annals of neurology May 1991 - 469-73 p. digital

Publication Type: Case Reports; Journal Article

0364-5134

10.1002/ana.410290504 doi


Chromosomes, Human, Pair 20
DNA--analysis
Epilepsy--genetics
Family
Female
Genetic Linkage
Genetic Testing
Genotype
Humans
Infant, Newborn
Pedigree
Phenotype
Recombination, Genetic