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A Homozygous Mutation in the Tight-Junction Protein JAM3 Causes Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts
Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA
Division of Genetics, Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Department of Medicine, Children's Hospital Boston, Boston, MA 02115, USA
Pediatric Neurology Unit, Department of Neurology, Massachusetts General Hospital, Boston, MA 02114, USA
Division of Genetics, Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Department of Medicine, Children's Hospital Boston, Boston, MA 02115, USA
Division of Genetics, Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Department of Medicine, Children's Hospital Boston, Boston, MA 02115, USA
Division of Genetics, Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Department of Medicine, Children's Hospital Boston, Boston, MA 02115, USA
Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA
Division of Genetics, Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Department of Medicine, Children's Hospital Boston, Boston, MA 02115, USA
Division of Genetics, Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Department of Medicine, Children's Hospital Boston, Boston, MA 02115, USA
Division of Genetics, Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Department of Medicine, Children's Hospital Boston, Boston, MA 02115, USA
Division of Genetics, Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Department of Medicine, Children's Hospital Boston, Boston, MA 02115, USA
Division of Genetics, Manton Center for Orphan Disease Research and Howard Hughes Medical Institute, Department of Medicine, Children's Hospital Boston, Boston, MA 02115, USA