Haubenwallner_1993_Genomics_18_392

Reference

Title : A novel missense mutation in the gene for lipoprotein lipase resulting in a highly conservative amino acid substitution (Asp180-->Glu) causes familial chylomicronemia (type I hyperlipoproteinemia) - Haubenwallner_1993_Genomics_18_392
Author(s) : Haubenwallner S , Horl G , Shachter NS , Presta E , Fried SK , Hofler G , Kostner GM , Breslow JL , Zechner R
Ref : Genomics , 18 :392 , 1993
Abstract : Haubenwallner_1993_Genomics_18_392
ESTHER : Haubenwallner_1993_Genomics_18_392
PubMedSearch : Haubenwallner_1993_Genomics_18_392
PubMedID: 8288243
Gene_locus related to this paper: human-LPL
Glu) causes familial chylomicronemia (type I hyperlipoproteinemia)
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Related information

Gene_locus related to this paper: human-LPL

Citations formats

Haubenwallner S, Horl G, Shachter NS, Presta E, Fried SK, Hofler G, Kostner GM, Breslow JL, Zechner R (1993)
A novel missense mutation in the gene for lipoprotein lipase resulting in a highly conservative amino acid substitution (Asp180-->Glu) causes familial chylomicronemia (type I hyperlipoproteinemia)
Genomics 18 :392

Haubenwallner S, Horl G, Shachter NS, Presta E, Fried SK, Hofler G, Kostner GM, Breslow JL, Zechner R (1993)
Genomics 18 :392