[Lecithin-cholesterol acyltransferase deficiency and fish eye disease].
作者信息
Gotoda T
出版信息
Ryoikibetsu Shokogun Shirizu. 1998(19 Pt 2):100-3.
PMID:9645018
Abstract
摘要
相似文献
1
[Lecithin-cholesterol acyltransferase deficiency and fish eye disease].
Ryoikibetsu Shokogun Shirizu. 1998(19 Pt 2):100-3.
2
[Fish eye disease revealing a partial LCAT deficiency].[鱼眼病揭示部分卵磷脂胆固醇酰基转移酶缺乏症]
Rev Med Interne. 2005 Jun;26(6):518-9. doi: 10.1016/j.revmed.2004.11.010. Epub 2004 Dec 16.
3
4
[LCAT (lecithin:cholesterol acyltransferase)].[卵磷脂胆固醇酰基转移酶（LCAT）]
Rinsho Byori. 2001 Nov;Suppl 116:125-30.
5
Corneal and macular manifestations in a case of deficient lecithin: cholesterol acyltransferase.
Jpn J Ophthalmol. 2004 Jan-Feb;48(1):82-4. doi: 10.1007/s10384-003-0007-1.
6
Lecithin-cholesterol acyltransferase (LCAT) deficiency without mutations in the coding sequence: a case report and literature review.编码序列无突变的卵磷脂胆固醇酰基转移酶（LCAT）缺乏症：一例报告及文献综述
Clin Nephrol. 2011 Oct;76(4):323-8. doi: 10.5414/cn106484.
7
LCAT deficiency as a cause of proteinuria and corneal opacification.卵磷脂胆固醇酰基转移酶缺乏症作为蛋白尿和角膜混浊的一个病因。
BMJ Case Rep. 2018 Mar 13;2018:bcr-2017-224129. doi: 10.1136/bcr-2017-224129.
8
[LCAT deficiency: a nephrological diagnosis].[卵磷脂胆固醇酰基转移酶缺乏症：一种肾脏科诊断]
G Ital Nefrol. 2011 Jul-Aug;28(4):369-82.
9
[Familial LCAT deficiency].[家族性卵磷脂胆固醇酰基转移酶缺乏症]
Nihon Rinsho. 1994 Dec;52(12):3210-5.
10
Gene symbol: LCAT. Disease: Fish eye disease.基因符号：LCAT。疾病：鱼眼病。
Hum Genet. 2004 Nov;115(6):533.
Zotero 插件