Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease.
作者信息
Maury C P, Kere J, Tolvanen R, de la Chapelle A
机构信息
Fourth Department of Medicine, University of Helsinki, Finland.
出版信息
Genomics. 1992 Jul;13(3):902-3. doi: 10.1016/0888-7543(92)90183-s.
PMID:1322360
Abstract
摘要
Zotero 插件