Mechanisms of disease: psychomotor retardation and high T-3 levels caused by 
mutations in monocarboxylate transporter 8.

Friesema, E. C. H.; Jansen, J.; Heuer, H.; Trajkovic, M.; Bauer, K.; Visser, T. J.

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Mechanisms of disease: psychomotor retardation and high T-3 levels caused by mutations in monocarboxylate transporter 8.

Friesema, E. C. H., Jansen, J., Heuer, H., Trajkovic, M., Bauer, K., & Visser, T. J. (2006). Mechanisms of disease: psychomotor retardation and high T-3 levels caused by mutations in monocarboxylate transporter 8. Nature Clinical Practice Endocrinology and Metabolism, 2(9), 512-523.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0012-E405-E Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0027-DC71-5

Genre: Journal Article

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Friesema, E. C. H., Author
Jansen, J., Author
Heuer, H., Author
Trajkovic, M., Author
Bauer, K.¹, Author
Visser, T. J., Author

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1Department of Molecular Developmental Biology, MPI for biophysical chemistry, Max Planck Society, ou_578590

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Free keywords: brain development; deiodinases; thyroid hormone; transporter; X-linked psychomotor retardation

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Language(s): eng - English

Dates: Date issued: 2006-09

Publication Status: Issued

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Identifiers: eDoc: 430546

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Title: Nature Clinical Practice Endocrinology and Metabolism

Source Genre: Journal

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Pages: - Volume / Issue: 2 (9) Sequence Number: - Start / End Page: 512 - 523 Identifier: -