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May 9, 1995Proceedings of the National Academy of SciencesOpen Access

A mutation in the promoter of the lipoprotein lipase (LPL) gene in a patient with familial combined hyperlipidemia and low LPL activity.

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Authors

WYWenbo YangUniversity of IowaDNDavid NevinUniversity of the WitwatersrandRPReiling PengUniversity of Washington

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Implication

Single LPL promoter variant finding warrants no practice change; leaves open its broader role in FCHL.

Key Points

Key points are not available for this paper at this time.

Cite This Study

Yang et al. (1995) studied this question.

synapsesocial.com/papers/6a6f23ba22b3175134db417bhttps://doi.org/10.1073/pnas.92.10.4462
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