X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locus.
作者信息
Mensink E J, Thompson A, Sandkuyl L A, Kraakman M E, Schot J D, Espanol T, Schuurman R K
出版信息
Hum Genet. 1987 May;76(1):96-9. doi: 10.1007/BF00283057.
PMID:2883112
Abstract
The gene involved in X-linked immunodeficiency with hyperimmunoglobulinemia M (XHM) was localized by the use of nine restriction fragment length polymorphic (RFLP) markers covering the entire X chromosome. Multipoint linkage analysis of RFLP data obtained in a three generation XHM pedigree indicates the Xq24-q27 area around the DXS42 RFLP locus as the most likely localization of the XHM locus.
摘要
Zotero 插件