Gene Locus : human-LPL
Mode of mutation : Natural mutant
Disease : Hyperlipoproteinemia TypeI
Summary :
AAA Change :
Allelic Variant :
Risk Factor :
Inhibitor :
Structure :
Disease by interaction :
Interact Gene Locus :
Xenobiotic sensitivity :
Modification :
Torpedo_number : No torpedo number
Kinetic Parameter : No kinetic parameter
News : No news
Comment :
T83del (T56 in mature protein) c.247_249+1del 4-bp ACGG deletion at the 3' boundary of exon 2
Title : Novel LPL mutations associated with lipoprotein lipase deficiency: two case reports and a literature review - Rahalkar_2009_Can.J.Physiol.Pharmacol_87_151 |
Author(s) : Rahalkar AR , Giffen F , Har B , Ho J , Morrison KM , Hill J , Wang J , Hegele RA , Joy T |
Ref : Canadian Journal of Physiology & Pharmacology , 87 :151 , 2009 |
Abstract : |
PubMedSearch : Rahalkar_2009_Can.J.Physiol.Pharmacol_87_151 |
PubMedID: 19295657 |
Gene_locus related to this paper: human-LPL |