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Article

[Presymptomatic DNA diagnosis of spinocerebellar ataxia type 1].

Genetika - 1 May 1997

Illarioshkin S N, Ivanova-Smolenskaia I A, Limborskaia S A, Ovchinnikov I V, Markova E D, Slominskiĭ P A, Kliushnikov S A, Miklina N I

Abstract excerpt

Hereditary autosomal dominant ataxias is a clinically and genetically heterogeneous group of diseases characterized by a progressive ataxia combined with the signs of multisystem involvement of the brain and spinal cord. The modern classification of these disorders of the central nervous system is based on recent advances in molecular genetics. In a form of dominant ataxia, spinocerebellar ataxia type 1 (SCA1),...

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PMID: 9273319

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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