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Autosomal recessive late onset multisystem disorder with cerebellar cortical atrophy at necropsy: report of a family.

A sister and brother developed a progressive syndrome comprising bulbar palsy, supranuclear ophthalmoplegia, facial impassivity, and cerebellar ataxia together with a mixed pyramidal and extrapyramidal deficit in the limbs, in the fourth decade of life. Their parents were unaffected and inheritance...

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Bibliografski detalji
Glavni autori: Harding, A E, Diengdoh, J V, Lees, A J
Format: Artigo
Jezik:Inglês
Izdano: 1984
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1027951/
https://ncbi.nlm.nih.gov/pubmed/6470726
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