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
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| Description | scientific article published in January 2004 |
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author: Berenice Bilharinho Mendonça |
| Publication date | January 1, 2004 |
| Language | English |
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