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Sirs: Spinocerebellar ataxia type 4 (SCA4) was first described in a large family of Scandinavian origin from Utah and is linked to chromosome 16q22.1 . The clinical phenotype is characterized by progressive cerebellar ataxia in combination with sensory axonal neuropathy. A second family was reported from Germany, the SCA4 candidate region could be refined to a 3.69 cM interval (7.94 Mb) [2–4]. Meanwhile, the gene locus responsible for a pure cerebellar ataxia in six Japanese families was mapped to the same region [5–7].
FingerprintDive into the research topics of 'Spinocerebellar ataxia type 4 and 16q22.1-linked Japanese ataxia are not allelic'. Together they form a unique fingerprint.
- 1 Finished
01.01.03 → 31.12.09
Project: DFG Funding