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	1.	Structure-based analysis of five novel disease-causing mutations in 21-hydroxylase-deficient patients. [electronic resource] by Minutolo, Carolina Nadra, Alejandro D Fernández, Cecilia Taboas, Melisa Buzzalino, Noemí Casali, Bárbara Belli, Susana Charreau, Eduardo H Alba, Liliana Dain, Liliana Producer: 20110802 In: PloS one vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency. [electronic resource] by Keselman, Ana Claudia Martin, Ayelen Scaglia, Paula Alejandra Sanguineti, Nora María Armando, Romina Gutiérrez, Mariana Braslavsky, Débora Ballerini, María Gabriela Ropelato, María Gabriela Ramirez, Laura Landi, Estefanía Domené, Sabina Castro, Julia F Cassinelli, Hamilton Casali, Bárbara Del Rey, Graciela Barros, Ángel Campos Nevado Blanco, Julián Domené, Horacio Jasper, Héctor Arberas, Claudia Rey, Rodolfo A Lapunzina-Badía, Pablo Bergadá, Ignacio Pennisi, Patricia A Producer: 20191129 In: European journal of endocrinology vol. 181 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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