Screening of mutations in congenital and isolated central hypothyroidism

ABSTRACT: Candidate gene sequencing of patients with congenital or isolated familial hypothyroidism.

INSTRUMENT(S): -

ORGANISM(S): Homo Sapiens

SUBMITTER: University of Turku, Biomedicine 

PROVIDER: PRJEB45041 | EVA | 2021-05-21

REPOSITORIES: EVA