New publication: Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency

Ziemnicka K, Budny B, Drobnik K, Baszko-Błaszyk D, Stajgis M, Katulska K, Waśko R, Wrotkowska E, Słomski R, Ruchała M
J. Appl. Genet., 2016 AUg;57(3):373-81, Epub 2015 Nov 25; IF 1.929; MNiSW 20

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