JASReference:Xiong WJ:Li WH:Posner I:Yamamura T:Yamamoto A:Gotto AM Jr:Chan L:,Am J Hum Genet,1991,48,383: Difference between revisions
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{{JASReference|mutation= | {{JASReference|mutation= | ||
&&APOC2/Del/70/C&&Q24fsX17&&exon3&&Del/108/C&& | &&APOC2/Del/70/C&&Q24fsX17&&exon3&&Del/108/C&&Q24fsX17&&exon3 | ||
|title=No severe bottleneck during human evolution: evidence from two apolipoprotein C-II deficiency alleles | |title=No severe bottleneck during human evolution: evidence from two apolipoprotein C-II deficiency alleles | ||
|doi= | |doi= | ||
|pmid=1990844 | |pmid=1990844 | ||
|comment=The article reports Japanese and Venezuelan patients with an identical phenotype of 17-amino acid frameshifted phenotype, caused by C deletion at codon 23 or 24. | |||
}} | }} | ||
Latest revision as of 23:19, 9 June 2013
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| Title | No severe bottleneck during human evolution: evidence from two apolipoprotein C-II deficiency alleles |
| Author(s) | (Click a name to see records for each author.) |
| Journal | American Journal of Human Genetics (2 pages) |
| Year | 1991 |
| Volume | 48 |
| Page | 383 |
The article reports Japanese and Venezuelan patients with an identical phenotype of 17-amino acid frameshifted phenotype, caused by C deletion at codon 23 or 24.
Genetic mutations in this article
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This database is maintained by the subcommittee for Lipid Metabolism in Japan Atherosclerosis Society. If you volunteer to contribute, please contact arita AT k.u-tokyo.ac.jp. |
このデータベースは日本動脈硬化学会 脂質代謝部会が作成しています。入力等に協力していただける方は有田 arita AT k.u-tokyo.ac.jp までご連絡下さい。 |
- Format of the page
The format of the page title is here. The format of mutation information is here. |
