spinocerebellar ataxia, autosomal recessive 3 selections

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General
Database Correlations
References

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spinocerebellar ataxia, autosomal recessive 3; spinocerebellar ataxia with blindness & deafness (SACR3)

Genetics: - 6p23-p21 Clinical manifestations: - features of spinocerebellar ataxia - optic & cochlear degeneration leading to blindness & deafness

General

spinocerebellar ataxia, autosomal recessive

Database Correlations

OMIM 271250

References

OMIM :accession 271250