Delineation of Novel Monogenic Disorders in the United Arab Emirates Population

NCT03589079 · clinicaltrials.gov ↗

UNKNOWN

Status

150

Enrollment

OTHER

Sponsor class

Conditions

Mendelian Disorders
Genetic Disorder
Novel Mutation
Hereditary Disorder
De Novo Mutation
Inherited Disease
Single-Gene Defects

Interventions

GENETIC: Sanger and/or Next Generation Sequencing (NGS)

Sponsor

Imperial College London Diabetes Centre