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Questioning the Association of the STMN2 Dinucleotide Repeat With Amyotrophic Lateral Sclerosis.
Ross, Jay P; Akçimen, Fulya; Liao, Calwing; Spiegelman, Dan; Weisburd, Ben; Dupré, Nicolas; Dion, Patrick A; Rouleau, Guy A; Farhan, Sali M K.
Afiliación
  • Ross JP; Department of Human Genetics (J.P.R., F.A., C.L., G.A.R., S.M.K.F.), Montreal Neurological Institute and Hospital (J.P.R., F.A., C.L., D.S., P.A.D., G.A.R., S.M.K.F.), and Department of Neurology and Neurosurgery (D.S., P.A.D., G.A.R., S.M.K.F.), McGill University, Montréal, Quebec, Canada; Program
  • Akçimen F; Department of Human Genetics (J.P.R., F.A., C.L., G.A.R., S.M.K.F.), Montreal Neurological Institute and Hospital (J.P.R., F.A., C.L., D.S., P.A.D., G.A.R., S.M.K.F.), and Department of Neurology and Neurosurgery (D.S., P.A.D., G.A.R., S.M.K.F.), McGill University, Montréal, Quebec, Canada; Program
  • Liao C; Department of Human Genetics (J.P.R., F.A., C.L., G.A.R., S.M.K.F.), Montreal Neurological Institute and Hospital (J.P.R., F.A., C.L., D.S., P.A.D., G.A.R., S.M.K.F.), and Department of Neurology and Neurosurgery (D.S., P.A.D., G.A.R., S.M.K.F.), McGill University, Montréal, Quebec, Canada; Program
  • Spiegelman D; Department of Human Genetics (J.P.R., F.A., C.L., G.A.R., S.M.K.F.), Montreal Neurological Institute and Hospital (J.P.R., F.A., C.L., D.S., P.A.D., G.A.R., S.M.K.F.), and Department of Neurology and Neurosurgery (D.S., P.A.D., G.A.R., S.M.K.F.), McGill University, Montréal, Quebec, Canada; Program
  • Weisburd B; Department of Human Genetics (J.P.R., F.A., C.L., G.A.R., S.M.K.F.), Montreal Neurological Institute and Hospital (J.P.R., F.A., C.L., D.S., P.A.D., G.A.R., S.M.K.F.), and Department of Neurology and Neurosurgery (D.S., P.A.D., G.A.R., S.M.K.F.), McGill University, Montréal, Quebec, Canada; Program
  • Dupré N; Department of Human Genetics (J.P.R., F.A., C.L., G.A.R., S.M.K.F.), Montreal Neurological Institute and Hospital (J.P.R., F.A., C.L., D.S., P.A.D., G.A.R., S.M.K.F.), and Department of Neurology and Neurosurgery (D.S., P.A.D., G.A.R., S.M.K.F.), McGill University, Montréal, Quebec, Canada; Program
  • Dion PA; Department of Human Genetics (J.P.R., F.A., C.L., G.A.R., S.M.K.F.), Montreal Neurological Institute and Hospital (J.P.R., F.A., C.L., D.S., P.A.D., G.A.R., S.M.K.F.), and Department of Neurology and Neurosurgery (D.S., P.A.D., G.A.R., S.M.K.F.), McGill University, Montréal, Quebec, Canada; Program
  • Rouleau GA; Department of Human Genetics (J.P.R., F.A., C.L., G.A.R., S.M.K.F.), Montreal Neurological Institute and Hospital (J.P.R., F.A., C.L., D.S., P.A.D., G.A.R., S.M.K.F.), and Department of Neurology and Neurosurgery (D.S., P.A.D., G.A.R., S.M.K.F.), McGill University, Montréal, Quebec, Canada; Program
  • Farhan SMK; Department of Human Genetics (J.P.R., F.A., C.L., G.A.R., S.M.K.F.), Montreal Neurological Institute and Hospital (J.P.R., F.A., C.L., D.S., P.A.D., G.A.R., S.M.K.F.), and Department of Neurology and Neurosurgery (D.S., P.A.D., G.A.R., S.M.K.F.), McGill University, Montréal, Quebec, Canada; Program
Neurol Genet ; 8(4): e678, 2022 Aug.
Article en En | MEDLINE | ID: mdl-35923349
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Neurol Genet Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Neurol Genet Año: 2022 Tipo del documento: Article