Congenital Secondary Hypothyroidism Caused by Exon Skipping due to a Homozygous Donor Splice Site Mutation in the TSHβ-Subunit Gene
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| Description | scientific article published on January 1, 2002 |
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| Publication date | January 1, 2002 |
| Language | English |
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https://academic.oup.com/jcem/article-pdf/87/1/336/9158345/jcem0336.pdf |
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| Missing/wrong data? | Edit Wikidata item |