Case of pachydermoperiostosis with solute carrier organic anion transporter family, member 2A1 (SLCO2A1) mutations

被引：5
|
作者：
Minakawa, Satoko [1 ]
Kaneko, Takahide [1 ]
Niizeki, Hironori [2 ]
Mizukami, Hiroki [3 ]
Saito, Yoko [4 ]
Nigawara, Takeshi [5 ]
Kurose, Rie [6 ]
Nakabayashi, Kazuhiko [7 ]
Kabashima, Kenji [8 ]
Sawamura, Daisuke [1 ]
机构：
[1] Hirosaki Univ, Grad Sch Med, Dept Dermatol, Hirosaki, Aomori 0368562, Japan
[2] Natl Ctr Child Hlth & Dev, Dept Dermatol, Tokyo, Japan
[3] Hirosaki Univ, Grad Sch Med, Dept Pathol & Mol Med, Hirosaki, Aomori 0368562, Japan
[4] Hirosaki Univ, Grad Sch Med, Dept Radiol Life Sci, Hirosaki, Aomori 0368562, Japan
[5] Hirosaki Univ, Grad Sch Med, Dept Endocrinol & Metab, Hirosaki, Aomori 0368562, Japan
[6] Hirosaki Univ, Grad Sch Med, Dept Orthopaed Surg, Hirosaki, Aomori 0368562, Japan
[7] Natl Res Inst Child Hlth & Dev, Dept Maternal Fetal Biol, Tokyo, Japan
[8] Kyoto Univ, Grad Sch Med, Dept Dermatol, Kyoto 606, Japan
来源：
JOURNAL OF DERMATOLOGY | 2015年 / 42卷 / 09期
关键词：
PRIMARY HYPERTROPHIC OSTEOARTHROPATHY; GENE;
D O I：
10.1111/1346-8138.12974
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
引用
收藏
页码：908 / 910
页数：3
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