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 (Q44695299)
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scientific article published in January 2004
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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 |
scientific article published in January 2004 |
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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 (English)
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Alexander A L Jorge
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Silvia C A L Souza
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Ivo J P Arnhold
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1 January 2004
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