A novel CIAS1 mutation in a Japanese patient with chronic infantile neurological cutaneous and articular syndrome

Hidetoshi Takada, Koichi Kusuhara, Akihiko Nomura, Shoichi Ohga, Mikiko Hayashi, Masutaka Furue, Toshiro Hara

Research output: Contribution to journalArticle

5 Citations (Scopus)
Original languageEnglish
Pages (from-to)785-786
Number of pages2
JournalEuropean Journal of Pediatrics
Volume164
Issue number12
DOIs
Publication statusPublished - Dec 1 2005

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Cryopyrin-Associated Periodic Syndromes
Craniofacial Abnormalities
Neurocutaneous Syndromes
Carrier Proteins
Skin
Mutation

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health

Cite this

A novel CIAS1 mutation in a Japanese patient with chronic infantile neurological cutaneous and articular syndrome. / Takada, Hidetoshi; Kusuhara, Koichi; Nomura, Akihiko; Ohga, Shoichi; Hayashi, Mikiko; Furue, Masutaka; Hara, Toshiro.

In: European Journal of Pediatrics, Vol. 164, No. 12, 01.12.2005, p. 785-786.

Research output: Contribution to journalArticle

Takada, Hidetoshi ; Kusuhara, Koichi ; Nomura, Akihiko ; Ohga, Shoichi ; Hayashi, Mikiko ; Furue, Masutaka ; Hara, Toshiro. / A novel CIAS1 mutation in a Japanese patient with chronic infantile neurological cutaneous and articular syndrome. In: European Journal of Pediatrics. 2005 ; Vol. 164, No. 12. pp. 785-786.
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