The characterization of hereditary abnormalities of keratin: Clouston's ectodermal dysplasia.
The characterization of hereditary abnormalities of keratin: Clouston's ectodermal dysplasia.
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角蛋白遗传性异常的特征：克劳斯顿外胚层发育不良。
DOI：
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发表时间：
1971
期刊：
影响因子：
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通讯作者：
Scriver Cr
中科院分区：
文献类型：
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作者：
Reynolds Jm;Gol'dberg Mb;Scriver Cr
：克劳斯顿型外胚层发育不良是一种由单剂量常染色体显性基因引起的疾病。它似乎只涉及皮肤及其附属器。对这种疾病中毛发蛋白的物理和化学异常的研究开始揭示相关基因的作用。
: Ectodermal dysplasia of the Clouston type is a disease caused by a single dose of an autosomal dominant gene. It appears to involve only the skin and its appendages. An investigation of the physical and chemical abnormalities of the hair protein in this disease is beginning to throw some light on the action of the gene involved.