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Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene
by
Rabacchi, Claudio, PhD
,
D'Addato, Sergio, MD
,
Palmisano, Silvia, MD
,
Lucchi, Tiziano, MD
,
Bertolini, Stefano, MD
,
Calandra, Sebastiano, MD
,
Tarugi, Patrizia, PhD
Published in
Journal of clinical lipidology
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Journal Of Clinical Lipidology
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Adult
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Base Sequence
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Cardiovascular
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Codon, Nonsense
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Familial Chylomicronemia
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Female
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Glycosylphosphatidylinositol-Anchored High-Density Lipoprotein-Binding Protein 1
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Homozygote
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Humans
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Hyperlipoproteinemia Type I - Diagnosis
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Hyperlipoproteinemia Type I - Genetics
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Hypertriglyceridemia
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Incidental Findings
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Life Sciences & Biomedicine
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Male
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Middle Aged
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Mutation, Missense
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Pancreatitis
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Pedigree
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Pharmacology & Pharmacy
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