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Spinocerebellar ataxia type 7: Report of an Indian family
Spinocerebellar ataxia type 7 (SCA7) is a form of autosomal dominant cerebellar ataxia which is associated with pigmentary retinal degeneration. It is known for its world-wide rarity except in the Scandinavian countries. It is very rarely reported from India and the neighbouring Asian countries. The...
Bewaard in:
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Medknow Publications & Media Pvt Ltd
2013
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3841638/ https://ncbi.nlm.nih.gov/pubmed/24339617 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0972-2327.120455 |
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