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Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
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Molybdenum cofactor deficiency-phenotypic variability in a family with a late-onset variant

E F Hughes1, L Fairbanks, H A Simmonds

  • 1Department of Paediatric Neurology, Newcomen Centre, Guy's Hospital, London, UK.

Developmental Medicine and Child Neurology
|February 12, 1998
PubMed

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