Gene Identification in Alternating Hemiplegia
Researchers at Georg Augustus University Gottingen, Germany studied the genetics of alternating hemiplegia of childhood (AHC) in 24 patients aged 8-35 years, using whole-exome sequencing to identify de novo mutations associated with the disease.
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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2012-09-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/506 |