Nonsense mutation in ADAM10 (p.tyr167*) associated with familial Alzheimer's disease: a clinical correlate of alfa-secretase haploinsufficiency


Por: Aguero, P, Artiga, M, Garcia-Ayllon, M, Saez J, Tellez, R, Guerrero-Lopez, R, Perez-Perez, J, Jimenez-Escrig, A and Gomez-Tortosa, E

Publicada: 1 may 2020
Resumen:


Filiaciones:
Artiga, M:
 Fdn Jimenez Diaz, Neurol, Madrid, Spain

:
 Univ Miguel Hernandez, Inst Neurocieneias Alicante, Alicante, Spain

Saez J:
 Univ Miguel Hernandez, Inst Neurocieneias Alicante, Alicante, Spain

Tellez, R:
 Hosp Univ Fdn Jimenez Diaz, Inmunol, Madrid, Spain

Guerrero-Lopez, R:
 Fdn Jimenez Diaz Hosp, Neurol Genet, Mdrid, Spain

Perez-Perez, J:
 Secugen SL, Madrid, Spain

Gomez-Tortosa, E:
 Fdn Jimenez Diaz, Neurol, Madrid, Spain
ISSN: 14681331





EUROPEAN JOURNAL OF NEUROLOGY
Editorial
Blackwell Publishing Inc., 111 RIVER ST, HOBOKEN 07030-5774, NJ USA, Reino Unido
Tipo de documento: Meeting Abstract
Volumen: 27 Número:
Páginas: 524-525
WOS Id: 000534616801315

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