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Pharmacologic correction of dominant-negative GH1 deficiency causing mutations.
Clin Transl Sci. 2011 Jun;4(3):175-9. doi: 10.1111/j.1752-8062.2011.00290.x.
Clin Transl Sci. 2011.
PMID: 21707947
Free PMC article.
A molecular basis for variation in clinical severity of isolated growth hormone deficiency type II.
Hamid R, Phillips JA 3rd, Holladay C, Cogan JD, Austin ED, Backeljauw PF, Travers SH, Patton JG.
Hamid R, et al.
J Clin Endocrinol Metab. 2009 Dec;94(12):4728-34. doi: 10.1210/jc.2009-0746. Epub 2009 Oct 16.
J Clin Endocrinol Metab. 2009.
PMID: 19837935
Free PMC article.
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