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

Sofía Siffo, Ezequiela Adrover, Cintia E. Citterio, Mirta Miras, Viviana Balbi, Ana Chiesa, Jacques Weill, Gabriela Sobrero, Verónica Gómez González, Patricia Papendieck,

Molecular and Cellular Endocrinology · 2017 · 31 citations · 65 references

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65

Primary structure of human thyroglobulin deduced from the sequence of its 8448-base complementary DNA

Yves Malthièry, Serge Lissitzky · European Journal of Biochemistry · 1987 · 325 citations

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Primary structure of bovine thyroglobulin deduced from the sequence of its 8,431-base complementary DNA

Luc Mercken, Marie-Jeanne Simons, Stéphane Swillens et al. · Nature · 1985 · 276 citations

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A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidism.

Tamio Ieiri, Pascale Cochaux, Héctor M. Targovnik et al. · Journal of Clinical Investigation · 1991 · 169 citations · Full text

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Up to date with human thyroglobulin

S.A. van de Graaf, Carrie Ris‐Stalpers, Erwin Pauws et al. · Journal of Endocrinology · 2001 · 150 citations · Full text

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Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones.

Geraldo Medeiros‐Neto, Pan Suk Kim, Sung Eun Yoo et al. · Journal of Clinical Investigation · 1996 · 132 citations · Full text

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