Identification of single-nucleotide polymorphisms in the human LPIN1 gene

Abstract

AbstractBecause mutations in the murine analog of human LPIN1 cause lipodystrophy in mice, LPIN1 is a candidate gene for human lipodystrophy syndromes. To identify possible disease mutations and/or common single-nucleotide polymorphisms (SNPs), we developed primer pairs to amplify the 21 exons of LPIN1. We used these primer pairs to sequence LPIN1 in… (More)
DOI: 10.1007/s100380200052

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