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Atherosclerosis
Volume 146, Issue 1
, Pages
141-151
, September 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
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PII: S0021-9150(99)00112-4
© 1999 Elsevier Science Ireland Ltd. All rights reserved.
« Previous
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Atherosclerosis
Volume 146, Issue 1
, Pages
141-151
, September 1999
