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Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism

Christian P Schaaf1, Manuel L Gonzalez-Garay, Fan Xia

  • 11] Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA. [2] Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, Texas, USA. [3].

Nature Genetics
|October 1, 2013
PubMed

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