Publication | Open Access

Novel compound heterozygous Thyroglobulin mutations c.745+1G>A/c.7036+2T>A associated with congenital goiter and hypothyroidism in a Vietnamese family. Identification of a new cryptic 5′ splice site in the exon 6

BiologyGenetic DisorderNatural SciencesGeneticsThyroid DiseaseMolecular BiologyMolecular GeneticsCongenital GoiterGenomicsThyroid HormoneExon 6MedicineSplice Site