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Paper Report for: Teh_1999_Atherosclerosis_146_141

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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 EM, Chisholm JW, Dolphin PJ, Pouliquen Y, Savoldelli M, De Gennes JL, Benlian P
Ref: Atherosclerosis, 146:141, 1999 : PubMed

        



Related information

Mutation | T138fsX144_human-LCAT,



Citations formats

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: 141-51

Teh EM, Chisholm JW, Dolphin PJ, Pouliquen Y, Savoldelli M, De Gennes JL, Benlian P (1999)
Atherosclerosis 146: 141-51



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