Kopp P

References (3)

Title : The p.A2215D thyroglobulin gene mutation leads to deficient synthesis and secretion of the mutated protein and congenital hypothyroidism with wide phenotype variation - Pardo_2009_J.Clin.Endocrinol.Metab_94_2938
Author(s) : Pardo V , Vono-Toniolo J , Rubio IG , Knobel M , Possato RF , Targovnik HM , Kopp P , Medeiros-Neto G
Ref : J Clinical Endocrinology Metab , 94 :2938 , 2009
Abstract :
PubMedSearch : Pardo_2009_J.Clin.Endocrinol.Metab_94_2938
PubMedID: 19509106
Gene_locus related to this paper: human-TG

Title : Naturally occurring mutations in the thyroglobulin gene - Vono-Toniolo_2005_Thyroid_15_1021
Author(s) : Vono-Toniolo J , Rivolta CM , Targovnik HM , Medeiros-Neto G , Kopp P
Ref : Thyroid , 15 :1021 , 2005
Abstract :
PubMedSearch : Vono-Toniolo_2005_Thyroid_15_1021
PubMedID: 16187910

Title : Thyroglobulin gene mutations and other genetic defects associated with congenital hypothyroidism - Vono-Toniolo_2004_Arq.Bras.Endocrinol.Metabol_48_70
Author(s) : Vono-Toniolo J , Kopp P
Ref : Arq Bras Endocrinol Metabol , 48 :70 , 2004
Abstract :
PubMedSearch : Vono-Toniolo_2004_Arq.Bras.Endocrinol.Metabol_48_70
PubMedID: 15611820
Gene_locus related to this paper: human-TG