| Literature DB >> 9176854 |
S Oikawa1, A Matsunaga, T Saito, H Sato, T Seki, K Hoshi, K Hayasaka, H Kotake, H Midorikawa, A Sekikawa, S Hara, K Abe, T Toyota, H Jingami, H Nakamura, J Sasaki.
Abstract
Lipoprotein glomerulopathy (LPG) is a novel disease characterized by proteinuria, lipoprotein thrombi in the glomeruli, and increased concentration of plasma apolipoprotein (apo) E. It is believed that a genetic disorder of apo E may be present and associated with the disease. Three patients with LPG were examined in this study. The patients' DNA sequences were analyzed, and a nucleotide G to C point mutation in exon 4 of the apo E gene was confirmed in each patient. This missense mutation denotes amino acid substitution of the proline residue for arginine residue at position 145 of apo E. This variant (apo E Sendai) may cause a marked molecular conformational change of the apo E. These findings suggest that a novel variant is etiologically related to LPG.Entities:
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Year: 1997 PMID: 9176854 DOI: 10.1681/ASN.V85820
Source DB: PubMed Journal: J Am Soc Nephrol ISSN: 1046-6673 Impact factor: 10.121