Report for Savoldelli M

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References (1)

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

Report for Savoldelli M

General

References (1)

1. 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