Title : Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144 - Teh_1999_Atherosclerosis_146_141 |
Author(s) : Teh EM , Chisholm JW , Dolphin PJ , Pouliquen Y , Savoldelli M , De Gennes JL , Benlian P |
Ref : Atherosclerosis , 146 :141 , 1999 |
Abstract : Teh_1999_Atherosclerosis_146_141 |
ESTHER : Teh_1999_Atherosclerosis_146_141 |
PubMedSearch : Teh_1999_Atherosclerosis_146_141 |
PubMedID: 10487497 |
Teh EM, Chisholm JW, Dolphin PJ, Pouliquen Y, Savoldelli M, De Gennes JL, Benlian P (1999)
Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144
Atherosclerosis
146 :141
Teh EM, Chisholm JW, Dolphin PJ, Pouliquen Y, Savoldelli M, De Gennes JL, Benlian P (1999)
Atherosclerosis
146 :141