Report for Ferrarini E

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References (1)

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