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
- INNDSUi006-A
- SCTCi043-A
- SCTCi043-A-1
- SCTCi043-A-1
- SCTCi044-A
- SCTCi044-A-1
- SCTCi044-A-1
- SCTCi045-A
- SCTCi045-A-1
- SCTCi045-A-1
- SCVIi134-A
- SCVIi137-A