Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism-Reference-Cited by-同舟云学术

Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism

Published:2018-09 Issue: Volume:473 Page:1-16
ISSN:0303-7207
Container-title:Molecular and Cellular Endocrinology
language:en
Short-container-title:Molecular and Cellular Endocrinology

Author:

Siffo Sofia,Adrover Ezequiela,Citterio Cintia E.,Miras Mirta B.,Balbi Viviana A.,Chiesa Ana,Weill Jacques,Sobrero Gabriela,González Verónica G.,Papendieck Patricia,Martinez Elena Bueno,Gonzalez-Sarmiento Rogelio,Rivolta Carina M.,Targovnik Héctor M.

Funder

FONCyT-ANPCyT-MINCyT

CONICET

Universidad de Buenos Aires

Publisher

Elsevier BV

Subject

Endocrinology,Molecular Biology,Biochemistry

Reference86 articles.

1. Detection of T.G. and TO genes compound mutations associated with thyroid carcinoma, toxic goiter and hypothyroidism in Iraqi patients;Abdul-Hassan;J. Med. Sci.,2013

2. Disorders of thyroid morphogenesis;Abu-Khudir;Best Pract. Res. Clin. Endocrinol. Metab.,2017

3. Congenital hypothyroidism caused by a novel homozygous mutation in the thyroglobulin gene;Agretti;Eur. J. Pediatr.,2013