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McCune–Albright syndrome: description of three clinical cases, features of diagnostics and treatment
Autor:
L. Ya. Rozhinskaya, D. G. Sardaeva, N. Y. Kalinchenko, A. M. Chukanova, N. V. Tarbaeva, S. A. Buryakina, V. P. Vladimirova, Z. E. Belaya, G. A. Melnichenko
Publikováno v:
Osteoporosis and Bone Diseases. 24:19-32
McCune Albright syndrome (MAS) is a rare disorder caused by a sporadic postzygotic mutation in the GNAS gene, which encodes the alpha subunit of the Gs signaling protein.Permanent activation of the Gs protein leads to uncontrolled production of intra