Advances and Perspectives in Genetics of Congenital Thyroid Disorders Associated with Thyroglobulin Gene Mutations
<p>Dyshormonogenesis due to thyroglobulin (TG) gene mutations is a rare cause of congenital hypothyroidism with an estimated incidence of approximately 1 in 100,000 newborns. The TG gene is organized in 48 exons, spanning over 270 kb on human chromosome 8q24. The human TG mRNA is 8.5 Kb long a...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Open Journal of Biological Sciences - Peertechz Publications,
2016-12-19.
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| Online Access: | Connect to this object online. |
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