Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS.
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A. Tsatsoulis | G. Hendy | H. Jüppner | M. Bastepe | A. Rosenbloom | R. Josse | J. Crawford | A. Slyper | J. Körkkö | L. Fröhlich | H. Koshiyama | J. Nakamoto | O. Indridason | T. Sugimoto