{"title":"Sialidosis, a new type of inborn disease.","authors":"G Strecker, J C Michalski","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>We describe the biochemical findings concerning five different types of mucolipidosis which have been defined as sialidosis on the basis of the specific enzyme deficiency and the nature of the storage material.</p>","PeriodicalId":72742,"journal":{"name":"Current problems in clinical biochemistry","volume":" 9","pages":"370-82"},"PeriodicalIF":0.0000,"publicationDate":"1979-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current problems in clinical biochemistry","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
We describe the biochemical findings concerning five different types of mucolipidosis which have been defined as sialidosis on the basis of the specific enzyme deficiency and the nature of the storage material.
分享
京公网安备 11010802042870号
京ICP备2023020795号-1
求助内容：
应助结果提醒方式：
扫码关注我们
