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Expanding Phenotype of VRK1 Mutations in Motor Neuron Disease

OBJECTIVE: In the past decade, hereditary forms of motor neuron disease (spinal muscular atrophy and/or amyotrophic lateral sclerosis) are increasingly identified. As advanced genetic testing is performed, molecular diagnosis can be obtained. Identifying new gene mutations can lead to further unders...

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Detalhes bibliográficos
Publicado no:J Clin Neuromuscul Dis
Main Authors: Nguyen, Thy P., Biliciler, Suur, Wiszniewski, Wojciech, Sheikh, Kazim
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4829393/
https://ncbi.nlm.nih.gov/pubmed/26583493
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/CND.0000000000000096
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