A unique point mutation in the NSDHL gene in a Japanese patient with CHILD syndrome

التفاصيل البيبلوغرافية
العنوان: A unique point mutation in the NSDHL gene in a Japanese patient with CHILD syndrome
المؤلفون: Kaoru Murata, Masaaki Yamazaki, Hiroshi Shinkai, Yasuhito Fukuzumi, Atsushi Hatamochi, Satoshi Ishikiriyama
المصدر: Journal of Dermatological Science. 33:67-69
بيانات النشر: Elsevier BV, 2003.
سنة النشر: 2003
مصطلحات موضوعية: Genetics, NSDHL gene, business.industry, Point mutation, Medicine, Dermatology, CHILD syndrome, business, medicine.disease, Molecular Biology, Biochemistry
تدمد: 0923-1811
DOI: 10.1016/s0923-1811(03)00151-8
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::d173ac949bda5149137702d2a500b9fd
https://doi.org/10.1016/s0923-1811(03)00151-8
Rights: CLOSED
رقم الانضمام: edsair.doi...........d173ac949bda5149137702d2a500b9fd
قاعدة البيانات: OpenAIRE
الوصف
تدمد:09231811
DOI:10.1016/s0923-1811(03)00151-8