Diagnostics and procedures are provided for detecting myotonic dystrophy in humans. The diagnostics and procedures are based on the detection of a CTG trinucleotide repeat in a variable length polymorphism of the myotonic dystrophy gene derived from the region of human chromosome 19q13 containing the myotonic dystrophy locus.
申请公布号
DE69313829(D1)
申请公布日期
1997.10.16
申请号
DE1993613829
申请日期
1993.02.18
申请人
UNIVERSITY OF OTTAWA, OTTAWA, ONTARIO, CA
发明人
KORNELUK, ROBERT, G., OTTAWA, ON, K1G 2L8, CA;MAHADEVAN, MANI, S., NEPEAN, ON, K2G 4C3, CA
