Associated Papers
A nonsynonymous TNFRSF11A variation increases NFκB activity and the severity of Paget's disease.
Gianfrancesco F et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research, 2012
Clinical and genetic findings in Hungarian patients with X-linked juvenile retinoschisis.
Lesch B et al.
Molecular Vision, 2008
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