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J-GLOBAL ID：201902215063308884   Reference number：19S1243780

Nevoid basal cell carcinoma syndrome caused by splicing mutations in the PTCH1 gene

Author (13)： Kato, Chise (Department of Molecular Genetics, Kitasato University Graduate School of Medical Sciences) ,  Arai, Yuto (Department of Molecular Genetics, Kitasato University Graduate School of Medical Sciences) ,  Nagao, Kazuaki (Department of Molecular Genetics, Kitasato University Graduate School of Medical Sciences) ,  Nagao, Kazuaki (Department of Molecular Genetics, Kitasato University School of Medicine) ,  Takayama, Yoshinaga (Department of Molecular Genetics, Kitasato University Graduate School of Medical Sciences) ,  Takayama, Yoshinaga (Department of Molecular Genetics, Kitasato University School of Medicine) ,  Kameyama, Kouzou (Department of Molecular Genetics, Kitasato University Graduate School of Medical Sciences) ,  Kameyama, Kouzou (Department of Molecular Genetics, Kitasato University School of Medicine) ,  Miyashita, Toshiyuki (Department of Molecular Genetics, Kitasato University Graduate School of Medical Sciences) ,  Miyashita, Toshiyuki (Department of Molecular Genetics, Kitasato University School of Medicine) ,  Fujii, Kentaro (Department of Molecular Genetics, Kitasato University School of Medicine) ,  Hatsuse, Hiromi (Department of Molecular Genetics, Kitasato University School of Medicine) ,  Fujii, Katsunori (Department of Pediatrics, Chiba University Graduate School of Medicine)
Material： Familial Cancer
Volume： 16  Issue： 1  Page： 131-138  Publication year： 2017 
JST Material Number： SCOPUS  ISSN： 1389-9600  CODEN： FCAAA 
Country of issue： Netherlands (NLD)  Language： English (EN)