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This page is a summary of: The first homozygous mutation (S226I) in the highly‐conserved WSXWS‐like motif of the GH receptor causing Laron syndrome: supression of GH secretion by GnRH analogue therapy not restored by dihydrotestosterone administration, Clinical Endocrinology, December 2003, Wiley,
DOI: 10.1111/j.1365-2265.2004.01930.x.
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