Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
Hyung‐Goo KimMolecular Neurogenetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02114, USAIngo KurthInstitut für Humangenetik, Universitätsklinikum Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, GermanyFei LanDepartment of Pathology, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USAIrene MelicianiFaculty of Science, University "La Sapienza," Piazzale Aldo Moro 5, 00185 Roma, ItalyWolfgang WenzelSoo Hyun EomDepartment of Life Science, Cell Dynamics Research Center, Gwangju Institute of Science and Technology, Gwangju 500-712, South KoreaGil Bu KangDepartment of Life Science, Cell Dynamics Research Center, Gwangju Institute of Science and Technology, Gwangju 500-712, South KoreaGeorg RosenbergerInstitut für Humangenetik, Universitätsklinikum Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, GermanyMustafa TekinDivision of Clinical Molecular Pathology and Genetics, Department of Pediatrics, Ankara University School of Medicine, Ankara, 06100 TurkeyMetin ÖzataGATA Haydarpasa Training Hospital, Department of Endocrinology, Istanbul, 34660 TurkeyDavid BickDivision of Medical Genetics, Departments of Pediatrics and Obstetrics & Gynecology, Medical College of Wisconsin, Milwaukee, WI 53226, USARichard J. SherinsSteven L. WalkerNeuroscience Program, The Medical College of Georgia, 1120 15th Street, Augusta, GA 30912, USAYang ShiDepartment of Pathology, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USAJames F. GusellaMolecular Neurogenetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02114, USALawrence C. LaymanThe Medical College of Georgia, 1120 15th Street, Augusta, GA 30912, USA
2008en
ABI
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