Two Exon-Skipping Mutations as the Molecular Basis of Succinic Semialdehyde Dehydrogenase Deficiency (4-Hydroxybutyric Aciduria)
- 1 August 1998
- journal article
- case report
- Published by Elsevier in American Journal of Human Genetics
- Vol. 63 (2) , 399-408
- https://doi.org/10.1086/301964
Abstract
No abstract availableKeywords
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