[Carrier detection and gene analysis in a Duchenne muscular dystrophy family].
作者信息
Lu F M
机构信息
Department of Medical Genetics, Harbin Medical University.
出版信息
Zhonghua Shen Jing Jing Shen Ke Za Zhi. 1990 Aug;23(4):231-3, 255.
PMID:1979269
Abstract
Probe C7, pERT87-15, 754 which on the short arm of the X chromosome are used in the linkage analysis of a DMD family by the use of restriction fragment length porlymorphism (RFLP) and serum CPK, CPK-MB are detected. Three obligated carriers are determined and we also find a deletion to pERT87-15 in this family.
摘要
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