UnknownNot applicableNCT03810859

Non-syndromic Inherited Anomalies of Mineralized Tooth Tissues: a Whole Exome Study to Identify New Pathogenic Variants

Studying Amelogenesis imperfecta

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Key facts

Sponsor
Assistance Publique - Hôpitaux de Paris
Principal Investigator
Céline GAUCHER, MD
APHP
Intervention
Blood sample(biological)
Enrollment
14 enrolled
Eligibility
4 years · All sexes
Timeline
2019 – 2022

Study locations (1)

Collaborators

French rare diseases Healthcare Network · The French Foundation for Rare Diseases

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT03810859 on ClinicalTrials.gov

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