Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects

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Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects Empty Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects

Post  Jon Moulton on Mon Jul 18, 2016 3:10 pm

Simon AJ, Lev A, Zhang Y, Weiss B, Rylova A, Eyal E, Kol N, Bare O, Cesarkas K, Soudack M, Greenberg-Kushnir N, Rhodes M, Wiest DL, Schiby G, Barshack I, Katz S, Pras E, Poran H, Reznik-Wolf H, Ribakovsky E, Simon C, Hazou W, Sidi Y, Lahad A, Katzir H, Sagie S, Aqeilan HA, Glousker G, Amariglio N, Tzfati Y, Selig S, Rechavi G, Somech R. Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects. J Exp Med. 2016;[Epub ahead of print] doi:10.1084/jem.20151618
Jon Moulton
Jon Moulton

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