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Genetic and cellular basis of cerebral cavernous malformations: implications for clinical management

✍ Scribed by S Bacigaluppi; SF Retta; S Pileggi; M Fontanella; L Goitre; L Tassi; A La Camera; A Citterio; MC Patrosso; G Tredici; S Penco


Book ID
119981565
Publisher
John Wiley and Sons
Year
2013
Tongue
English
Weight
522 KB
Volume
83
Category
Article
ISSN
0009-9163

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Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare and severe arrhythmogenic disorder. Although usually transmitted in a recessive form, few cases of dominant mutations have been reported. Thirteen mutations in the CASQ2 gene have been reported so far in association with CPVT. We