p.L571P in the linker domain of rat thyroglobulin causes intracellular retention-Reference-Cited by-同舟云学术

p.L571P in the linker domain of rat thyroglobulin causes intracellular retention

Published:2020-04 Issue: Volume:505 Page:110719
ISSN:0303-7207
Container-title:Molecular and Cellular Endocrinology
language:en
Short-container-title:Molecular and Cellular Endocrinology

Author:

Citterio Cintia E.,Siffo Sofia,Moya Christian M.,Pio Mauricio Gomes,Molina Maricel F.,Scheps Karen G.,Rey Osvaldo A.,Arvan Peter,Rivolta Carina M.,Targovnik Héctor M.

Funder

Fondo para la Investigación Científica y Tecnológica

Consejo Nacional de Investigaciones Científicas y Técnicas

Universidad de Buenos Aires

National Institutes of Health

American Thyroid Association

Publisher

Elsevier BV

Subject

Endocrinology,Molecular Biology,Biochemistry

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4. Congenital hypothyroidism with goitre caused by new mutations in the thyroglobulin gene;Caputo;Clin. Endocrinol. (Oxf),2007

5. Compound heterozygous mutations in the thyroglobulin gene (1143delC and 6725G>A[R2223H]) resulting in fetal goitrous hypothyroidism;Caron;J. Clin. Endocrinol. Metab.,2003

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