Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Génétique des Maladies du Développement, |
RCV001004662 | SCV001164111 | likely pathogenic | Autosomal dominant nocturnal frontal lobe epilepsy 5 | 2015-10-28 | criteria provided, single submitter | clinical testing |