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Recent advances in understanding dominant spinocerebellar ataxias from clinical and genetic points of view
Abstract Spinocerebellar ataxias (SCAs) are rare types of cerebellar ataxia with a dominant mode of inheritance. To date, 47 SCA subtypes have been identified, and the number of genes implicated in SCAs is continually increasing. Polyglutamine (polyQ) expansion diseases ( ATXN1/SCA1, ATXN2/SCA2, ATX...
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| Foilsithe in: | F1000Res |
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| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
F1000 Research Limited
2018
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6234732/ https://ncbi.nlm.nih.gov/pubmed/30473770 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.15788.1 |
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