Coexistence of two different pseudohypoparathyroidism subtypes (Ia and Ib) in the same kindred with independent Gsα coding mutations and GNAS imprinting defects

B. Lecumberri, E. Fernández-Rebollo, L. Sentchordi, P. Saavedra, A. Bernal-Chico, L. F. Pallardo, J. M. Jiménez Bustos, L. Castaño, M. De Santiago, O. Hiort, Guiomar Pérez De Nanclares*, Murat Bastepe

*Corresponding author for this work
37 Citations (Scopus)

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