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MCT8 mutation analysis and identification of the first femal…
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression.
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression.
Article, Chapter
Authors: S.G. Frints
Publication: European Journal of Human Genetics, Volume:16, Issue:9, Page(s):1029-1037
ISSN: 1018-4813
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View Full Text Source:European Journal of Human Genetics,European Journal of Human Genetics,Springer Complete Journals Opens in new Window
Journal:  European Journal of Human Genetics Source:Springer Complete Journals Opens in new Window
Collection:  Springer Complete Journals Opens in new Window
Coverage:
  • 1993-01-01~present; volume:1~present;issue:1~present
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