myotonic dystrophy type 1

Description

Steinert disease, also known as myotonic dystrophy type 1, is a muscle disease characterized by myotonia and by multiorgan damage that combines various degrees of muscle weakness, arrhythmia and/or cardiac conduction disorders, cataract, endocrine damage, sleep disorders and baldness.

Cell Lines

CBRCULi002-A
CBRCULi003-A
CBRCULi004-A
CBRCULi005-A
CBRCULi007-A
CBRCULi018-A
CBRCULi019-A
CBRCULi020-A
CENSOi008-A
CHUQi001-A
HADe001-A
HADe006-A
KCLe014-A
RGIe057-A
RGIe061-A
VUBe003-A
ZZUi015-A
CBRCULi012-A
CBRCULi013-A