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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Familial 6p22.2 duplication associates with mild developmental delay and increased SSADH activity

Linda Siggberg1, Aki Mustonen, Robert Schuit

  • 1Department of Pathology, Haartman Institute, University of Helsinki, Finland. linda.siggberg@helsinki.fi

American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics
|March 26, 2011
PubMed
Abstract

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