Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2
<p>Abstract</p> <p>Background</p> <p>The autosomal recessively inherited ataxia with oculomotor apraxia 2 (AOA2) is a neurodegenerative disorder characterized by juvenile or adolescent age of onset, gait ataxia, cerebellar atrophy, axonal sensorimotor neuropathy, oculom...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
BMC,
2009-09-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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