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Association between IL4 (–590), ACE (I)/(D), CCR5 (32), CTLA4 (+49) and IL1-RN (VNTR in intron 2) gene polymorphisms and vitiligo
European Journal of Dermatology, 03/09/09
Pehlivan S et al. - Vitiligo is a common skin disorder characterized by patterned depigmentation, because of a decrease of melanin pigment resulting from apparent melanocyte loss. CTLA4 and IL1-RN genes might play roles in the genetic etiology of vitiligo.
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Potential role of interleukin-17 in the pathogenesis of bullous pemphigoid
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Today in Basic Science/Genetics...keeping you current
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Genetic basis of oculocutaneous albinism
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Analysis of family history of palmoplantar hyperhidrosis in Japan
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The Effect of Aminolevulinic Acid Photodynamic Therapy on Microcomedones and Macrocomedones
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Therapy of Sezary syndrome
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Extramammary Pagets disease with intracytoplasmic lumen formation
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