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Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome |
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| Authors: | Kim Hyung-Goo Kurth Ingo Lan Fei Meliciani Irene Wenzel Wolfgang Eom Soo Hyun Kang Gil Bu Rosenberger Georg Tekin Mustafa Ozata Metin Bick David P Sherins Richard J Walker Steven L Shi Yang Gusella James F Layman Lawrence C |
| Affiliation: | 1 Molecular Neurogenetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02114, USA 2 Institut für Humangenetik, Universitätsklinikum Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany 3 Department of Pathology, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA 4 Faculty of Science, University “La Sapienza,” Piazzale Aldo Moro 5, 00185 Roma, Italy 5 Forschungszentrum Karlsruhe, Institute for Nanotechnology, PO Box 3640, 76021 Karlsruhe, Germany 6 Department of Life Science, Cell Dynamics Research Center, Gwangju Institute of Science and Technology, Gwangju 500-712, South Korea 7 Division of Clinical Molecular Pathology and Genetics, Department of Pediatrics, Ankara University School of Medicine, Ankara, 06100 Turkey 8 GATA Haydarpasa Training Hospital, Department of Endocrinology, Istanbul, 34660 Turkey 9 Division of Medical Genetics, Departments of Pediatrics and Obstetrics & Gynecology, Medical College of Wisconsin, Milwaukee, WI 53226, USA 10 Director of Andrology, Columbia Fertility Associates, Washington, DC 20037, USA 11 Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics & Gynecology; Reproductive Medicine and Developmental Neurobiology Programs in the Institute of Molecular Medicine and Genetics; The Medical College of Georgia, 1120 15th Street, Augusta, GA 30912, USA 12 Neuroscience Program, The Medical College of Georgia, 1120 15th Street, Augusta, GA 30912, USA |
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