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Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
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Persistent NKH with transient or absent symptoms and a homozygous GLDC mutation

Stanley H Korman1, Avihu Boneh, Akiko Ichinohe

  • 1Department of Clinical Biochemistry, Hadassah-Hebrew University Medical Center, Jerusalem, Israel. korman@hadassah.org.il

Annals of Neurology
|July 6, 2004
PubMed

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