Clinical and genetic characteristics of hereditary laminopathies
Naminopathies belong to a wide allelic series of diseases caused by mutations of one gene, LMNA, encoding for protein lamin A/C. Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive EmeryDreifuss muscular dystrophy, dilated cardiomyopathy 1A, familial partial lipodys...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Research Center of Neurology
2017-02-01
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| Series: | Анналы клинической и экспериментальной неврологии |
| Subjects: | |
| Online Access: | https://annaly-nevrologii.com/journal/pathID/article/viewFile/389/292 |