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Current Medical Research and Opinion, ISSN 0300-7995, 05/2019, Volume 35, Issue 5, pp. 925 - 925
Journal Article
Brain and Nerve, ISSN 1881-6096, 07/2013, Volume 65, Issue 7, pp. 811 - 823
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Clinical Neurology, ISSN 0009-918X, 05/2012, Volume 52, Issue 5, pp. 303 - 313
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 05/2018, Volume 63, Issue 5, pp. 687 - 690
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), caused by NOTCH3, primarily affects small cerebral... 
MOYAMOYA-DISEASE | RNF213 | GENE | DIAGNOSTIC-CRITERIA | GENETICS & HEREDITY
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Nature, ISSN 0028-0836, 12/2008, Volume 456, Issue 7222, pp. 611 - 616
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International Journal of Molecular Sciences, ISSN 1661-6596, 09/2015, Volume 16, Issue 9, pp. 21294 - 21309
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Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 11291 - 14
Fused in sarcoma (FUS) was identified as a component of typical inclusions in frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS).... 
Motor neurons | Phenotypes | Sarcoma | Myeloid leukemia | FUS gene | Amyotrophic lateral sclerosis | Sclerosis | Genotype & phenotype | FUS protein | Insects | Inclusion bodies | Morphology | Degeneration | Imaginal discs | Fusion protein | Frontotemporal dementia
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Neurological Sciences, ISSN 1590-1874, 08/2019, pp. 1 - 3
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American Journal of Medical Genetics Part A, ISSN 1552-4825, 03/2018, Volume 176, Issue 3, pp. 712 - 714
Journal Article