A novel mutation in intron 11 donor splice site, responsible of a rare genotype in thyroglobulin gene by altering the pre-mRNA splincing process. Cell expression and bioinformatic analysis-Reference-Cited by-同舟云学术

A novel mutation in intron 11 donor splice site, responsible of a rare genotype in thyroglobulin gene by altering the pre-mRNA splincing process. Cell expression and bioinformatic analysis

Published:2021-02 Issue: Volume:522 Page:111124
ISSN:0303-7207
Container-title:Molecular and Cellular Endocrinology
language:en
Short-container-title:Molecular and Cellular Endocrinology

Author:

Pio Mauricio Gomes,Molina Maricel F.,Siffo Sofia,Chiesa Ana^ORCID,Rivolta Carina M.,Targovnik Héctor M.^ORCID

Funder

Universidad de Buenos Aires

Fondo para la Investigación Científica y Tecnológica

Consejo Nacional de Investigaciones Científicas y Técnicas

Publisher

Elsevier BV

Subject

Endocrinology,Molecular Biology,Biochemistry

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4. Metastatic thyroid follicular carcinoma arising from congenital goiter due to a novel splice donor site mutation in the thyroglobulin gene;Alzahrani;J. Clin. Endocrinol. Metab.,2006

5. Digenic DUOX1 and DUOX2 mutations in cases with congenital hypothyroidism;Aycan;J. Clin. Endocrinol. Metabol.,2017

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