Report for Mauran PL

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References (2)

Title : Novel mutational mechanism in the thyroglobulin gene: imperfect DNA inversion as a cause for hereditary hypothyroidism - Citterio_2013_Mol.Cell.Endocrinol_381_220
Author(s) : Citterio CE , Rossetti LC , Souchon PF , Morales C , Thouvard-Viprey M , Salmon-Musial AS , Mauran PL , Doco-Fenzy M , Gonzalez-Sarmiento R , Rivolta CM , De Brasi CD , Targovnik HM
Ref : Mol Cell Endocrinol , 381 :220 , 2013
Abstract : Citterio_2013_Mol.Cell.Endocrinol_381_220
ESTHER : Citterio_2013_Mol.Cell.Endocrinol_381_220
PubMedSearch : Citterio_2013_Mol.Cell.Endocrinol_381_220
PubMedID: 23933148
Gene_locus related to this paper: human-TG

Title : Congenital goitre with hypothyroidism caused by a novel compound heterozygous mutations in the thyroglobulin gene - Targovnik_2010_Clin.Endocrinol.(Oxf)_72_716
Author(s) : Targovnik HM , Souchon PF , Machiavelli GA , Salmon-Musial AS , Mauran PL , Sulmont V , Doco-Fenzy M , Rivolta CM
Ref : Clinical Endocrinology (Oxf) , 72 :716 , 2010
Abstract : Targovnik_2010_Clin.Endocrinol.(Oxf)_72_716
ESTHER : Targovnik_2010_Clin.Endocrinol.(Oxf)_72_716
PubMedSearch : Targovnik_2010_Clin.Endocrinol.(Oxf)_72_716
PubMedID: 20447071
Gene_locus related to this paper: human-TG