A novel asparangine to aspartate (N132D) mutation in the The FOXE1 gene in congenital hypothyroidism

JUNIT, SARNI BINTI MAT (2005) A novel asparangine to aspartate (N132D) mutation in the The FOXE1 gene in congenital hypothyroidism. Hormone Research.

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Item Type: Other
Uncontrolled Keywords: A novel asparangine to aspartate (N132D) mutation in the The FOXE1 gene in congenital hypothyroidi
Subjects: R Medicine
Depositing User: MR. ADNAN YAHYA
Date Deposited: 11 Feb 2011
Last Modified: 11 Feb 2011
URI: http://repository.um.edu.my/id/eprint/9938

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