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Multiple café au lait spots in familial patients with MAP2K2 mutation
Authors:Toshiki Takenouchi  Atsushi Shimizu  Chiharu Torii  Rika Kosaki  Takao Takahashi  Hideyuki Saya  Kenjiro Kosaki
Affiliation:1. Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan;2. Department of Molecular Biology, Keio University School of Medicine, Tokyo, Japan;3. Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan;4. Division of Medical Genetics, National Center for Child Health and Development, Tokyo, Japan;5. Division of Gene Regulation, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan
Abstract:
Keywords:cafe au lait spots  rasopathies  MAP2K2  neurofibromatosis type 1  Noonan syndrome  neurofibromatosis–  Noonan syndrome
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