Author:
Olivati Caroline,Favilla Bianca Pereira,Freitas Erika Lopes,Santos Bibiana,Melaragno Maria Isabel,Meloni Vera Ayres,Piazzon Flavia
Funder
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Fundação de Amparo à Pesquisa do Estado de São Paulo
Subject
Endocrinology,Genetics,Molecular Biology
Reference19 articles.
1. Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study;Groeneweg;Lancet Diabetes Endocrinol.,2020
2. The MCT8 thyroid hormone transporter and Allan-Herndon-Dudley syndrome;Schwartz;Best Pract. Res. Clin. Endocrinol. Metab.,2007
3. Monocarboxylate transporters (SLC16): function, regulation, and role in health and disease;Felmlee;Pharmacol. Rev.,2020
4. Importance of monocarboxylate transporter 8 for the blood-brain barrier-dependent availability of 3,5,3′-triiodo-L-thyronine;Ceballos;Endocrinology,2009
5. MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression;Frints;Eur. J. Hum. Genet.,2008
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