Opening the window: The case for carrier and perinatal screening for spinal muscular atrophy.

Burns, Joseph K; Kothary, Rashmi; Parks, Robin J

Burns, Joseph K; Kothary, Rashmi; Parks, Robin J.

Affiliation

Burns JK; Regenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Canada; Department of Biochemistry, Microbiology, and Immunology, University of Ottawa, Ottawa, Canada; University of Ottawa Centre for Neuromuscular Disease, Ottawa, Canada.
Kothary R; Regenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Canada; University of Ottawa Centre for Neuromuscular Disease, Ottawa, Canada; Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Canada; Department of Medicine, University of Ottawa, Ottawa, Canada.
Parks RJ; Regenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Canada; Department of Biochemistry, Microbiology, and Immunology, University of Ottawa, Ottawa, Canada; University of Ottawa Centre for Neuromuscular Disease, Ottawa, Canada; Department of Medicine, University of Ottawa, Ottawa, Canada. Electronic address: rparks@ohri.ca.

Neuromuscul Disord ; 26(9): 551-9, 2016 09.

Article de En | MEDLINE | ID: mdl-27460292

Sujet(s)
Mots clés

Genetic screening; Spinal muscular atrophy; Therapy

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Amyotrophie spinale / Dépistage génétique Type d'étude: Diagnostic_studies / Prognostic_studies / Screening_studies Limites: Animals / Humans Langue: En Journal: Neuromuscul Disord Sujet du journal: NEUROLOGIA Année: 2016 Type de document: Article Pays d'affiliation: Canada

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