Associated Papers
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population.
Mahdieh N et al.
Human Genomics, 2024
Complete APTX deletion in a patient with ataxia with oculomotor apraxia type 1.
van Minkelen R et al.
Bmc Medical Genetics, 2015
26285866 (PubMed )
Supplement: 12881_2015_213_MOESM2_ESM.pdf
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