Autosomal recessive spastic paraplegias types 7 and 76
Introduction. Since 2017, the Research Centre for Medical Genetics has been conducting the first clinical and molecular study in Russia of a heterogeneous spastic paraplegia group based on the MPS high throughput sequencing method. Our group of molecularly diagnosed SPGs (types with known genes) inc...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
Research Center of Neurology
2021-06-01
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Series: | Анналы клинической и экспериментальной неврологии |
Subjects: | |
Online Access: | https://annaly-nevrologii.com/journal/pathID/article/viewFile/742/573 |