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

页码：908 / 910

页数：3

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