Development of the Tool " iPSC " for the Functional Study of Mutations Responsible for Mental Retardation

NCT02980302 · clinicaltrials.gov ↗

NA

Phase

COMPLETED

Status

4

Enrollment

OTHER

Sponsor class

Conditions

Intellectual Deficiency
Asymptomatic Carrier of the Mutation of the Gene MYT1L
Healthy Volunteers

Interventions

PROCEDURE: Cutaneous biopsy

Sponsor

University Hospital, Grenoble