Mutational analysis of 29 patients with autosomal-recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan

T. Takeichi; K. Tanahashi; T. Taki; M. Kono; K. Sugiura; M. Akiyama

doi:10.1111/bjd.15070

Mutational analysis of 29 patients with autosomal-recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan

T. Takeichi, K. Tanahashi, T. Taki, M. Kono, K. Sugiura, M. Akiyama

皮膚科学

研究成果: ジャーナルへの寄稿 › Letter › 査読

8 被引用数 (Scopus)

本文言語	英語
ページ（範囲）	290-292
ページ数	3
ジャーナル	British Journal of Dermatology
巻	177
号	1
DOI	https://doi.org/10.1111/bjd.15070
出版ステータス	出版済み - 07-2017

All Science Journal Classification (ASJC) codes

皮膚病学

文献へのアクセス

10.1111/bjd.15070

他のファイルとリンク

引用スタイル

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title = "Mutational analysis of 29 patients with autosomal-recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan",

author = "T. Takeichi and K. Tanahashi and T. Taki and M. Kono and K. Sugiura and M. Akiyama",

note = "Funding Information: Funding sources: The authors acknowledge financial support from Japan Society for the Promotion of Science KAKENHI grant numbers 15H04887, 15K15415, 15H06280 and 16K19717. The work was also supported by the Japan Intractable Diseases Research Foundation.",

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Mutational analysis of 29 patients with autosomal-recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan. / Takeichi, T.; Tanahashi, K.; Taki, T. その他.
In: British Journal of Dermatology, Vol. 177, No. 1, 07.2017, p. 290-292.

研究成果: ジャーナルへの寄稿 › Letter › 査読

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T2 - LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan

AU - Takeichi, T.

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AU - Taki, T.

AU - Kono, M.

AU - Sugiura, K.

AU - Akiyama, M.

N1 - Funding Information: Funding sources: The authors acknowledge financial support from Japan Society for the Promotion of Science KAKENHI grant numbers 15H04887, 15K15415, 15H06280 and 16K19717. The work was also supported by the Japan Intractable Diseases Research Foundation.

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