Questioning the causality of HTT CAG-repeat expansions in FTD/ALS.

Autor: Thomas Q; AP-HP, Genetic Department, University Hospital Pitié-Salpêtrière, Paris, France., Coarelli G; AP-HP, Genetic Department, University Hospital Pitié-Salpêtrière, Paris, France; Sorbonne University, Institut du Cerveau-Paris Brain Institute-ICM, INSERM, CNRS, Paris, France., Heinzmann A; AP-HP, Genetic Department, University Hospital Pitié-Salpêtrière, Paris, France; Sorbonne University, Institut du Cerveau-Paris Brain Institute-ICM, INSERM, CNRS, Paris, France., Le Ber I; Sorbonne University, Institut du Cerveau-Paris Brain Institute-ICM, INSERM, CNRS, Paris, France; AP-HP, National Reference center 'rare and young dementias,' IM2A, University Hospital Pitié-Salpêtrière, Paris, France., Amador MDM; AP-HP, Genetic Department, University Hospital Pitié-Salpêtrière, Paris, France; Sorbonne University, Department of Neurology, National Reference center ALS Paris, AP-HP, University Hospital Pitié-Salpêtrière, Paris, France., Durr A; AP-HP, Genetic Department, University Hospital Pitié-Salpêtrière, Paris, France; Sorbonne University, Institut du Cerveau-Paris Brain Institute-ICM, INSERM, CNRS, Paris, France. Electronic address: alexandra.durr@icm-institute.org.
Jazyk: angličtina
Zdroj: Neuron [Neuron] 2021 Jun 16; Vol. 109 (12), pp. 1945-1946.
DOI: 10.1016/j.neuron.2021.04.010
Databáze: MEDLINE