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Title:	Novel PNPLA2 gene mutations in Chinese Han patients causing neutral lipid storage disease with myopathy
Source:	Journal of Human Genetics [1434-5161] Lin, Pengfei yr:2012

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description	1.	Kaneko, K. "A novel mutation in PNPLA2 causes neutral lipid storage disease with myopathy and triglyceride deposit cardiomyovasculopathy: A case report and literature review." Neuromuscular disorders 24.7 (2014): 634-641.
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