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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Bibliographic Details
Main Author: J Gordon Millichap (Author)
Format: Book
Published: Pediatric Neurology Briefs Publishers, 2012-09-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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