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- 2009
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Mark
Novel pathogenic mechanism suggested by ex vivo analysis of MCT8 (SLC16A2) mutations
(
- Contribution to journal › Article
- 2007
-
Mark
Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine
(
- Contribution to journal › Article