Variable clinical phenotypes in a family with homozygous c.1159G>A mutation in the thyroid peroxidase gene.

HAN, HEH CHOON (2014) Variable clinical phenotypes in a family with homozygous c.1159G>A mutation in the thyroid peroxidase gene. Hormone Research in Paediatrics, 81. pp. 356-360.

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Item Type: Article
Uncontrolled Keywords: Variable clinical phenotypes in a family with homozygous c.1159G>A mutation in the thyroid peroxi
Subjects: R Medicine
Depositing User: MR. ADNAN YAHYA
Date Deposited: 11 Mar 2015
Last Modified: 11 Mar 2015
URI: http://repository.um.edu.my/id/eprint/98314

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