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Article

Phenotypic expression of benign familial neonatal convulsions linked to chromosome 20.

Archives of neurology - 1 Nov 1994

Berkovic S F, Kennerson M L, Howell R A, Scheffer I E, Hwang P A, Nicholson G A

Abstract excerpt

OBJECTIVES: To determine whether the syndrome of benign familial neonatal convulsions in a large family was linked to markers on chromosome 20q and to study the seizure patterns in affected individuals. DESIGN: A clinical and molecular biologic study of a single large family in which the probands were identical twins with benign familial neonatal convulsions. PATIENTS: Thirteen living affected family members and...

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Source

Identifiers

PMID: 7980108
DOI: 10.1001/archneur.1994.00540230063014

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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