Human Genome Epidemiology Literature Finder
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Query Trace: Parkinson Disease and CSMD1[original query] |
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Whole-exome sequencing associates novel CSMD1 gene mutations with familial Parkinson disease. Neurology. Genetics 2017 8 3 (5): e177. Ruiz-Martínez Javier, Azcona Luis J, Bergareche Alberto, Martí-Massó Jose F, Paisán-Ruiz Co |
- Page last reviewed:Feb 1, 2024
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