Agretti_2013_Eur.J.Pediatr_172_959

Reference

Title : Congenital hypothyroidism caused by a novel homozygous mutation in the thyroglobulin gene - Agretti_2013_Eur.J.Pediatr_172_959
Author(s) : Agretti P , De Marco G , Di Cosmo C , Ferrarini E , Montanelli L , Bagattini B , Vitti P , Tonacchera M
Ref : Eur J Pediatr , 172 :959 , 2013
Abstract : Agretti_2013_Eur.J.Pediatr_172_959
ESTHER : Agretti_2013_Eur.J.Pediatr_172_959
PubMedSearch : Agretti_2013_Eur.J.Pediatr_172_959
PubMedID: 23455760
Gene_locus related to this paper: human-TG

Related information

Gene_locus related to this paper: human-TG

Citations formats

Agretti P, De Marco G, Di Cosmo C, Ferrarini E, Montanelli L, Bagattini B, Vitti P, Tonacchera M (2013)
Congenital hypothyroidism caused by a novel homozygous mutation in the thyroglobulin gene
Eur J Pediatr 172 :959

Agretti P, De Marco G, Di Cosmo C, Ferrarini E, Montanelli L, Bagattini B, Vitti P, Tonacchera M (2013)
Eur J Pediatr 172 :959