DOI:
10.1055/s-00000017
Experimental and Clinical Endocrinology & Diabetes
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References
Reynaud R, Barlier A, Vallette-Kasic S. et al.
An uncommon phenotype with familial central hypogonadism caused by a novel PROP1 gene mutant truncated in the transactivation domain.
J Clin Endocrinol Metab 2005;
90: 4880-4887
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