Novel PRKAR1A gene mutations in Carney Complex

Carney complex is a syndrome that may include cardiac and mucocutaneous myxomas, spotting skin pigmentation, and endocrine lesions. Many patients with Carney complex have been shown to have a stop codon mutation in the PRKAR1A gene in the 17q22-24 region. Here we present the case of a 57 year-old ma...

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Bibliografiske detaljer
Main Authors: Pan, Lorraine, Peng, Lan, Jean-Gilles, J, Zhang, Ximin, Wieczorek, Rosemary, Jain, Shilpa, Levine, Vicki, Osman, Iman, Prieto, Victor G, Lee, Peng
Format: Artigo
Sprog:Inglês
Udgivet: e-Century Publishing Corporation 2010
Fag:
Case Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2897110/
https://ncbi.nlm.nih.gov/pubmed/20606737
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