(Q34109180)
Statements
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Congenital secondary hypothyroidism caused by exon skipping due to a homozygous donor splice site mutation in the TSHbeta-subunit gene (English)
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Joachim Pohlenz
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Alexandra Dumitrescu
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Ulrich Aumann
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Gerhard Koch
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Ralph Melchior
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Dirk Prawitt
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Samuel Refetoff
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1 January 2002
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87
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336-339
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Identifiers
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