TG Gene Mutations and Congenital Hypothyroidism
NCT00493103 · Status: COMPLETED · Type: OBSERVATIONAL
Last updated 2007-06-27
Summary
The aim of this study was to identify mutations in the thyroglobulin gene that might be present in patients with fetal goiter and congenital goiter hypothyroidism.
Conditions
- Congenital Hypothyroidism
Sponsors & Collaborators
-
Fundação de Amparo à Pesquisa do Estado de São Paulo
collaborator OTHER_GOV -
University of Sao Paulo
lead OTHER
Principal Investigators
-
Viviane Pardo · University of Sao Paulo
-
Geraldo Medeiros-Neto · University of Sao Paulo
Eligibility
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2003-07-31
- Completion
- 2007-06-30
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