Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22.
Progressive myoclonus epilepsy of Univerricht-Lundborg type is a clinically defined entity among the progressive myoclonus epilepsies. It is an autosomal recessive disorder. The underlying biochemical defect is unknown. We used linkage analysis to localize the gene in 12 families with the aid of pol...
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| Publicado no: | Proc Natl Acad Sci U S A |
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| Principais autores: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
1991
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC51519/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1673790/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.88.9.3696 |
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