Defining causal variants in rare epilepsies: an essential team effort between biomedical scientists, geneticists and epileptologists. (2022)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ejmg.2022.104531

PubMed Identifier: 35618197

Publication URI: http://europepmc.org/abstract/MED/35618197

Type: Journal Article/Review

Volume: 65

Parent Publication: European journal of medical genetics

Issue: 7

ISSN: 1769-7212