(Q21124576)
English
autosomal recessive spinocerebellar ataxia 19
human disease
- Lichtenstein-Knorr syndrome
- autosomal recessive spinocerebellar ataxia type 19
- Progressive autosomal recessive ataxia-sensorineural hearing loss syndrome
- SCAR19
- LICHTENSTEIN-KNORR SYNDROME; LIKNS
- LIKNS
- Progressive autosomal recessive ataxia-deafness syndrome
- Spinocerebellar Ataxia, Autosomal Recessive 19
Statements
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Identifiers
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