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Nature Genetics, ISSN 1061-4036, 11/2010, Volume 42, Issue 11, pp. 1021 - 1026
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2013, Volume 8, Issue 11, pp. e78496 - e78496
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Journal of Clinical Investigation, ISSN 0021-9738, 07/2011, Volume 121, Issue 7, pp. 2662 - 2667
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Journal of Neurology, ISSN 0340-5354, 7/2017, Volume 264, Issue 7, pp. 1520 - 1522
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s00415-017-8494-z 
Neurology | Neurosciences | Medicine & Public Health | Neuroradiology | EPISODIC ATAXIA | CLINICAL NEUROLOGY | MUTATION | FAMILY | Complications and side effects | Care and treatment | Carrier proteins | Ataxia | Development and progression | Genetic aspects | Seizures (Medicine) | Health aspects | Seizures
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NEUROLOGY, ISSN 0028-3878, 01/2018, Volume 90, Issue 3, pp. 142 - 143
Additional neurologic signs such as mild cerebellar ataxia and uncommon EEG and MRI findings in patients with generalized chorea and a positive family history... 
CAG REPEAT | CLINICAL NEUROLOGY | DRPLA
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Clinical and Translational Allergy, ISSN 2045-7022, 02/2019, Volume 9, Issue 1, pp. 9 - 9
Hereditary angioedema (HAE) is a life-threatening disease characterized by recurrent episodes of subcutaneous and mucosal swellings and abdominal cramping.... 
PROPHYLAXIS | PLASMA KALLIKREIN | ALLERGY | INHIBITOR | Histamine | Angioneurotic edema | Gene mutations | Genes | Tranexamic acid | Family | Thrombolytic drugs | Icatibant
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