Kelly Capuder

Years Active: 2017-2017
Publications (10 Years): 1

This page only lists publications with an associated author ORCID identifier.

Publications

Stefano Volpi, Yasuhiro Yamazaki, Patrick M Brauer, Ellen van Rooijen, Atsuko Hayashida, Anne Slavotinek, Hye Sun Kuehn, Maja Di Rocco, Carlo Rivolta, Ileana Bortolomai, Likun Du, Kerstin Felgentreff, Lisa Ott de Bruin, Kazutaka Hayashida, George Freedman, Genni Enza Marcovecchio, Kelly Capuder, Prisni Rath, Nicole Luche, Elliott J Hagedorn, Antonella Buoncompagni, Beryl Royer-Bertrand, Silvia Clara Giliani, Pietro Luigi Poliani, Luisa Imberti, A Kerry Dobbs, Fabienne E Poulain, Alberto Martini, John Manis, Robert J Linhardt, Marita Bosticardo, Sergio Damian Rosenzweig, Hane Lee, Jennifer M Puck, Juan-Carlos Zúñiga-Pflücker, Leonard I Zon, Pyong Woo Park, Andrea Superti-Furga, Luigi Daniele Notarangelo
EXTL3 mutations cause skeletal dysplasia, immune deficiency, and developmental delay. The Journal of experimental medicine 214 (3) (2017)

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