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 |