Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Sclerosis and CHRNB4[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 |
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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