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Paper Report for: Liu_2020_Front.Genet_11_741

Reference

Title: Analysis of a Chinese Pedigree With Familial Chylomicronemia Syndrome Reveals Two Novel LPL Mutations by Whole-Exome Sequencing
Liu Y, Lan Z, Zhao F, Zhang S, Zhang W
Ref: Front Genet, 11:741, 2020 : PubMed

        



Related information

Gene_Locus| human-LPL


Citations formats

Liu Y, Lan Z, Zhao F, Zhang S, Zhang W (2020)
Analysis of a Chinese Pedigree With Familial Chylomicronemia Syndrome Reveals Two Novel LPL Mutations by Whole-Exome Sequencing
Front Genet 11: 741

Liu Y, Lan Z, Zhao F, Zhang S, Zhang W (2020)
Front Genet 11: 741



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