A Novel Syndrome Combining Thyroid and Neurological Abnormalities Is Associated with Mutations in a Monocarboxylate Transporter Gene

Author:

Dumitrescu Alexandra M.,Liao Xiao-Hui,Best Thomas B.,Brockmann Knut,Refetoff Samuel

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference22 articles.

1. Thyroid hormone transporters: recent advances;Abe;Trends Endocrinol Metab,2002

2. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation;Allen;Am J Hum Genet,1992

3. Action of thyroid hormone in brain;Bernal;J Endocrinol Invest,2002

4. Biochemistry, cellular and molecular biology, and physiological roles of the iodothyronine selenodeiodinases;Bianco;Endocr Rev,2002

5. The expression of lactate transporters (MCT1 and MCT4) in heart and muscle;Bonen;Eur J Appl Physiol,2001

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