...酰胺酶(TGM1)ELISA试剂盒 角鲨烯单加氧酶(SQLE)ELISA试剂盒 角膜蛋白(KERA)ELISA试剂盒 角化粒(CDSN)ELISA试剂盒 角化蛋白(CNFN)ELISA试剂盒 角化不良蛋白(DKC)ELISA试剂盒 角蛋白9(KRT9)ELISA试剂盒 角蛋白81(KRT81)ELISA试剂盒 角蛋白8(KRT8)ELISA试剂盒 角...
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湿角化蛋白不同于表皮囊肿和皮样囊肿的成熟角化鳞状上皮。
"Wet" keratin is different from the mature (orthokeratotic) keratinous squames seen in epidermoid or dermoid cysts.
蛋白质太少会导致夜盲症，滤泡性角化过度，干眼症，幼儿发病率和死亡率增加。
Too few proteins lead to night blindness, perifollicular hyperkeratosis, xerophthalmia, increased morbidity and mortality in young children.
结论：角蛋白9基因的G485A突变是导致该家系发生弥漫性掌跖角化病的原因。
Conclusion the mutation G485A found in keratin 9 gene is the disease-causing mutation in the diffuse palmoplantar keratoderma family.
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