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

1. Lecumberri, B.
2. Fernández-Rebollo, E.
3. Sentchordi, L.
4. Saavedra, P.
5. Bernal-Chico, A.
6. Pallardo, L.F.
7. Jiménez Bustos, J.M.
8. Castaño, L.
9. De Santiago, M.
10. Hiort, O.
11. Pérez De Nanclares, G.
12. Bastepe, M.