Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Sclerosis and CHRNA4[original query] |
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Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. Human molecular genetics 2009 Oct 18 (20): 3997-4006. Sabatelli Mario, Eusebi Fabrizio, Al-Chalabi Ammar, Conte Amelia, Madia Francesca, Luigetti Marco, Mancuso Irene, Limatola Cristina, Trettel Flavia, Sobrero Fabrizia, Di Angelantonio Silvia, Grassi Francesca, Di Castro Amalia, Moriconi Claudia, Fucile Sergio, Lattante Serena, Marangi Giuseppe, Murdolo Marina, Orteschi Daniela, Del Grande Alessandra, Tonali Pietro, Neri Giovanni, Zollino Marcel |
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: the Italian multicentre study. Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2012 Oct 13 (6): 580-4. Sabatelli Mario, Lattante Serena, Conte Amelia, Marangi Giuseppe, Luigetti Marco, Del Grande Alessandra, Chiò Adriano, Corbo Massimo, Giannini Fabio, Mandrioli Jessica, Mora Gabriele, Calvo Andrea, Restagno Gabriella, Lunetta Christian, Penco Silvana, Battistini Stefania, Zeppilli Paolo, Bizzarro Alessandra, Capoluongo Ettore, Neri Giovanni, Rossini Paolo Maria, Zollino Marcel |
Exome Sequencing of a Portuguese Cohort of Frontotemporal Dementia Patients: Looking Into the ALS-FTD Continuum. Frontiers in neurology 2022 13 886379. Tábuas-Pereira Miguel, Santana Isabel, Gibbons Elizabeth, Paquette Kimberly, Almeida Maria Rosário, Baldeiras Inês, Bras Jose, Guerreiro Ri |
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