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Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
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Identification of two HEXA mutations causing infantile-onset Tay-Sachs disease in the Persian population

Alireza Haghighi1, Jamileh Rezazadeh, Azam Ahmadi Shadmehri

  • 1Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

Journal of Human Genetics
|July 29, 2011
PubMed

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