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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1974 | 2 |
2000 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 85502
3 results
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Homozygosity mapping of spinocerebellar ataxia with cerebellar atrophy and peripheral neuropathy to 9q33-34, and with hearing impairment and optic atrophy to 6p21-23.
Eur J Hum Genet. 2000 Dec;8(12):986-90. doi: 10.1038/sj.ejhg.5200586.
Eur J Hum Genet. 2000.
PMID: 11175288
Optic cochleovestibular degenerations in hereditary ataxias. II. Temporal bone pathology in two cases of Friedreich's ataxia with vestibulo-cochlear disorders.
Spoendlin H.
Spoendlin H.
Brain. 1974 Mar;97(1):41-8. doi: 10.1093/brain/97.1.41.
Brain. 1974.
PMID: 4434170
No abstract available.
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Optic and cochleovestibular degenerations in the hereditary ataxias. I. Clinico-pathological and genetic aspects.
van Bogaert L, Martin L.
van Bogaert L, et al.
Brain. 1974 Mar;97(1):15-40. doi: 10.1093/brain/97.1.15.
Brain. 1974.
PMID: 4154794
No abstract available.
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