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Nature, ISSN 0028-0836, 01/2004, Volume 427, Issue 6972, pp. 311 - 312
Journal Article
Brain & Development, ISSN 0387-7604, 2015, Volume 38, Issue 4, pp. 399 - 406
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BMC Genomics, ISSN 1471-2164, 09/2016, Volume 17, Issue 1
Background: Genome-wide CRISPR-Cas9 dropout screens can identify genes whose knockout affects cell viability. Recent CRISPR screens detected thousands of... 
NRAS | Driver mutations | Kinase | Negative selection | EGFR | Whole genome CRISPR screen | Dropout | CELLS | DISCOVERY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GROWTH | GENES | GENETICS & HEREDITY | Genome-wide association studies | Usage | Research | Gene mutations | Cancer cells
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PLoS ONE, ISSN 1932-6203, 12/2016, Volume 11, Issue 12, p. e0168215
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ORPHANET JOURNAL OF RARE DISEASES, ISSN 1750-1172, 07/2019, Volume 14, Issue 1, pp. 179 - 17
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Annals of Neurology, ISSN 0364-5134, 05/2016, Volume 79, Issue 5, pp. 826 - 840
Objective Mutations in the spastic paraplegia gene 11 (SPG11), encoding spatacsin, cause the most frequent form of autosomal‐recessive complex hereditary... 
CYTOKINESIS | DEFECTS | GENE | HEREDITARY SPASTIC PARAPLEGIA | PROLIFERATION | SPATACSIN | MUTATIONS | THIN CORPUS-CALLOSUM | SPG11 | NEUROSCIENCES | PROGRESSION | CLINICAL NEUROLOGY
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Journal Article
Stroke, ISSN 0039-2499, 02/2012, Volume 43, Issue 2, pp. 514 - 523
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Journal Article