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Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations.
Eur J Hum Genet. 2016 Mar;24(3):415-20. doi: 10.1038/ejhg.2015.126. Epub 2015 Jun 10.
Eur J Hum Genet. 2016.
PMID: 26059845
Free PMC article.
High prevalence of PROP1 defects in Lithuania: phenotypic findings in an ethnically homogenous cohort of patients with multiple pituitary hormone deficiency.
Navardauskaite R, Dusatkova P, Obermannova B, Pfaeffle RW, Blum WF, Adukauskiene D, Smetanina N, Cinek O, Verkauskiene R, Lebl J.
Navardauskaite R, et al.
J Clin Endocrinol Metab. 2014 Jan;99(1):299-306. doi: 10.1210/jc.2013-3090. Epub 2013 Dec 20.
J Clin Endocrinol Metab. 2014.
PMID: 24178788
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Mutations in PROP1 cause familial combined pituitary hormone deficiency.
Wu W, Cogan JD, Pfäffle RW, Dasen JS, Frisch H, O'Connell SM, Flynn SE, Brown MR, Mullis PE, Parks JS, Phillips JA 3rd, Rosenfeld MG.
Wu W, et al.
Nat Genet. 1998 Feb;18(2):147-9. doi: 10.1038/ng0298-147.
Nat Genet. 1998.
PMID: 9462743
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