A novel homozygous missense mutation in SLURP1 causes Mal de Meleda with an atypical phenotype

被引:0
|
作者
Gruber, R. [1 ]
Hennies, H. C. [2 ]
Romani, N. [1 ]
Schmuth, M. [1 ]
机构
[1] Innsbruck Med Univ, Dept Dermatol & Venereol, A-6020 Innsbruck, Austria
[2] Univ Cologne, Div Dermatogenet, Cologne, Germany
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暂无
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
P065
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页码:173 / 173
页数:1
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