دورية أكاديمية

Localized autosomal recessive epidermolysis bullosa simplex arising from a novel homozygous frameshift mutation in DST (BPAG1).

التفاصيل البيبلوغرافية
العنوان: Localized autosomal recessive epidermolysis bullosa simplex arising from a novel homozygous frameshift mutation in DST (BPAG1).
المؤلفون: Wen, D., Balacco, D. L., Bardhan, A., Harper, N., Walsh, D., Ryan, G., Liu, L., Guy, A., McGrath, J. A., Ogboli, M., Heagerty, A. H. M.
المصدر: Clinical & Experimental Dermatology; Feb2022, Vol. 47 Issue 2, p497-502, 6p, 1 Color Photograph, 1 Diagram, 1 Chart
مصطلحات موضوعية: FRAMESHIFT mutation, RECESSIVE genes, EPIDERMOLYSIS bullosa
مستخلص: Click https://wileyhealthlearning.com/#/online-courses/1bbce4bb-2328-4e18-8410-6773c8e4ac83 for the corresponding questions to this CME article. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:03076938
DOI:10.1111/ced.14917