Résultats de la recherche

Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

Pas de texte intégral

Crow Y, Chase D, Lowenstein Schmidt J, Szynkiewicz M, Forte G, Gornall H, Oojageer A, Anderson B, Pizzino A, Helman G, Abdel-Hamid M, Abdel-Salam G, Ackroyd S, Aeby A, Agosta G, Albin C, Allon-Shalev S, Arellano M, Ariaudo G, Aswani V, Babul-Hirji R, Baildam E, Bahi-Buisson N, Bailey K, Barnerias C, Barth M, Battini R, Beresford M, Bernard G, Bianchi M, Billette de Villemeur T, Blair E, Bloom M, Burlina A, Carpanelli M, Carvalho D, Castro-Gago M, Cavallini A, Cereda C, Chandler K, Chitayat D, Collins A, Sierra Corcoles C, Cordeiro N, Crichiutti G, Dabydeen L, Dale R, D'Arrigo S, De Goede C, De Laet C, De Waele L, Denzler I, Desguerre I, Devriendt K, Di Rocco M, Fahey M, Fazzi E, Ferrie C, Figueiredo A, Gener B, Goizet C, Gowrinathan N, Gowrishankar K, Hanrahan D, Isidor B, Kara B, Khan N, King M, Kirk E, Kumar R, Lagae L, Landrieu P, Lauffer H, Laugel Vincent, La Piana R, Lim M, Lin J, Linnankivi T, Mackay M, Marom D, Marques Lourenco C, McKee S, Moroni I, Morton J, Moutard M, Murray K, Nabbout R, Nampoothiri S, Nunez-Enamorado N, Oades P, Olivieri I, Ostergaard J, Perez-Duenas B, Prendiville J, Ramesh V, Rasmussen M, Regal L, Ricci F, Rio M, Rodriguez D, Roubertie A, Salvatici E, Segers K, Sinha G, Soler D, Spiegel R, Stodberg T, Straussberg R, Swoboda K, Suri M, Tacke U, Tan T, te Water Naude J, Wee Teik K, Thomas M, Till M, Tonduti D, Valente E, Van Coster R, van der Knaap M, Vassallo G, Vijzelaar R, Vogt J, Wallace G, Wassmer E, Webb H, Whitehouse W, Whitney R, Zaki M, Zuberi S, Livingston J, Rozenberg F, Lebon P, Vanderver A, Orcesi S, Rice G

Articles Scientifiques

2015

American Journal of Medical Genetics Part A

Laboratoire de Génétique Médicale - LGM - UMRS1112