未登录Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export
Legati, Andrea; Giovannini, Donatella; Nicolas, Gael; Lopez-Sanchez, Uriel; Quintans, Beatriz; Oliveira, Joao R. M.; Sears, Renee L.; Ramos, Eliana Marisa; Spiteri, Elizabeth; Sobrido, Maria-Jesus; Carracedo, Angel; Castro-Fernandez, Cristina; Cubizolle, Stephanie; Fogel, Brent L.; Goizet, Cyril; Jen, Joanna C.; Kirdlarp, Suppachok; Lang, Anthony E.; Miedzybrodzka, Zosia; Mitarnun, Witoon; Paucar, Martin; Paulson, Henry; Pariente, Jeremie; Richard, Anne-Claire; Salins, Naomi S.; Simpson, Sheila A.; Striano, Pasquale; Svenningsson, Per; Tison, Francois; Unni, Vivek K.; Vanakker, Olivier; Wessels, Marja W.; Wetchaphanphesat, Suppachok; Yang, Michele; Boller, Francois; Campion, Dominique; Hannequin, Dither; Sitbon, Marc; Geschwind, Daniel H.; Battini, Jean-Luc; Coppola, Giovanni
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收藏Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)
Oliveira, JRM; Spiteri, E; Sobrido, MJ; Hopfer, S; Klepper, J; Voit, T; Gilbert, J; Wszolek, ZK; Calne, DB; Stoessl, AJ; Hutton, M; Manyam, BV; Boller, F; Baquero, M; Geschwind, DH
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收藏Reporting clinical trials: full access to all the data
Rosenberg, RN; Aminoff, M; Boller, F; Soerensen, PS; Griggs, RC; Hachinski, V; Hallett, M; Johnson, RT; Kennard, C; Lang, AE; Lees, AJ; Lisak, R; Newsom-Davis, J; Pedley, TA; Selzer, ME; Zochodne, D
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收藏Reporting clinical trials - Full access to all the data
Rosenberg, RN; Aminoff, M; Boller, F; Sorensen, PS; Griggs, RC; Hachinski, V; Hallett, M; Johnson, RT; Kennard, C; Lang, AE; Lees, AJ; Lisak, R; Newsom-Davis, J; Pedley, TA; Selzer, ME; Zochodne, D
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收藏Reporting clinical trials: Full access to all the data
Rosenberg, RN; Aminoff, M; Boller, F; Soerensen, PS; Griggs, RC; Hallett, M; Hachinski, V; Johnson, RT; Kennard, C; Lang, AE; Lees, AJ; Lisak, R; Newsom-Davis, J; Pedley, TA; Selzer, ME; Zochodne, D
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