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)
scientific article published in January 2004
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(P31) (Q13442814)
(P50) (Q42957618)
(P304) 36-40
(P407) (Q1860)
(P433) 1
(P478) 60
(P577) Thursday, January 1, 2004
(P921) (Q669822)
(Q114049690)
(P1433) (Q15762781)
(P1476) "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" (language: en)
(P2093) Alexander A L Jorge
Silvia C A L Souza
Ivo J P Arnhold
(P2860) (Q38356819)
(Q47869149)
other details
description scientific article published in January 2004

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