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pubmed-article:15982496pubmed:abstractTextPRKAR1A gene encodes the type 1A regulatory subunit of protein kinase A. The mutation of this gene causes Carney complex which is an autosomal dominant multiple neoplasia syndrome characterized by spotty pigmentations, endocrine overactivity and cardiac myxoma. We hypothesized that cardiac myxoma may be associated with PRKAR1A gene mutation and determined whether mutation in the PRKAR1A gene is the cause of familial and sporadic cardiac myxoma.lld:pubmed
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pubmed-article:15982496pubmed:articleTitlePRKAR1A gene mutation in patients with cardiac myxoma.lld:pubmed
pubmed-article:15982496pubmed:affiliationMolecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Takara-machi 13-1, Kanazawa 920-8640, Japan. maboo398@hotmail.comlld:pubmed
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