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| 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 |
| Title : Familial lecithin:cholesterol acyltransferase deficiency: molecular analysis of a compound heterozygote: LCAT (Arg147 --> Trp) and LCAT (Tyr171 --> Stop) - Guerin_1997_Atherosclerosis_131_85 |
| Author(s) : Guerin M , Dachet C , Goulinet S , Chevet D , Dolphin PJ , Chapman MJ , Rouis M |
| Ref : Atherosclerosis , 131 :85 , 1997 |
| Abstract : Guerin_1997_Atherosclerosis_131_85 |
| ESTHER : Guerin_1997_Atherosclerosis_131_85 |
| PubMedSearch : Guerin_1997_Atherosclerosis_131_85 |
| PubMedID: 9180249 |