Longevity in untreated congenital growth hormone deficiency due to a homozygous mutation in the GHRH receptor gene.
Aguiar-Oliveira MH, Oliveira FT, Pereira RM, Oliveira CR, Blackford A, Valenca EH, Santos EG, Gois-Junior MB, Meneguz-Moreno RA, Araujo VP, Oliveira-Neto LA, Almeida RP, Santos MA, Farias NT, Silveira DC, Cabral GW, Calazans FR, Seabra JD, Lopes TF, Rodrigues EO, Porto LA, Oliveira IP, Melo EV, Martari M, Salvatori R.
Aguiar-Oliveira MH, et al. Among authors: pereira rm.
J Clin Endocrinol Metab. 2010 Feb;95(2):714-21. doi: 10.1210/jc.2009-1879. Epub 2009 Dec 4.
J Clin Endocrinol Metab. 2010.
PMID: 19965916
Free PMC article.