edoc

Items where Author is "Speck-Martins, Carlos E."

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Date | Item Type | Refereed
Jump to: 2021 | 2010
Number of items: 2.

2021

Allou, Lila and Balzano, Sara and Magg, Andreas and Quinodoz, Mathieu and Royer-Bertrand, Beryl and Schöpflin, Robert and Chan, Wing-Lee and Speck-Martins, Carlos E. and Carvalho, Daniel Rocha and Farage, Luciano and Lourenço, Charles Marques and Albuquerque, Regina and Rajagopal, Srilakshmi and Nampoothiri, Sheela and Campos-Xavier, Belinda and Chiesa, Carole and Niel-Bütschi, Florence and Wittler, Lars and Timmermann, Bernd and Spielmann, Malte and Robson, Michael I. and Ringel, Alessa and Heinrich, Verena and Cova, Giulia and Andrey, Guillaume and Prada-Medina, Cesar A. and Pescini-Gobert, Rosanna and Unger, Sheila and Bonafé, Luisa and Grote, Phillip and Rivolta, Carlo and Mundlos, Stefan and Superti-Furga, Andrea. (2021) Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulator. Nature, 592. pp. 93-98.

2010

Kennerson, Marina L. and Nicholson, Garth A. and Kaler, Stephen G. and Kowalski, Bartosz and Mercer, Julian F. B. and Tang, Jingrong and Llanos, Roxana M. and Chu, Shannon and Takata, Reinaldo I. and Speck-Martins, Carlos E. and Baets, Jonathan and Almeida-Souza, Leonardo and Fischer, Dirk and Timmerman, Vincent and Taylor, Philip E. and Scherer, Steven S. and Ferguson, Toby A. and Bird, Thomas D. and De Jonghe, Peter and Feely, Shawna M. E. and Shy, Michael E. and Garbern, James Y.. (2010) Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy. American journal of human genetics, Vol. 86, H. 3. pp. 343-352.

This list was generated on Thu Mar 28 16:28:58 2024 CET.