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Congenital Secondary Hypothyroidism Caused by Exon Skipping due to a Homozygous Donor Splice Site Mutation in the TSHβ-Subunit Gene
Pohlenz, Joachim, Dumitrescu, Alexandra, Aumann, Ulrich, Koch, Gerhard, Melchior, Ralph, Prawitt, Dirk, Refetoff, SamuelVolume:
87
Journal:
The Journal of Clinical Endocrinology & Metabolism
DOI:
10.1210/jcem.87.1.8154
Date:
January, 2002
File:
PDF, 287 KB
2002