Simultaneous hyper- and hypomethylation at imprinted loci in a subset of patients with gnas epimutations underlies a complex and different mechanism of multilocus methylation defect in pseudohypoparathyroidism type 1b

1. Maupetit-Méhouas, S.
2. Azzi, S.
3. Steunou, V.
4. Sakakini, N.
5. Silve, C.
6. Reynes, C.
7. Perez de Nanclares, G.
8. Keren, B.
9. Chantot, S.
10. Barlier, A.
11. Linglart, A.
12. Netchine, I.