A novel JAK3 mutation in a Japanese patient with severe combined immunodeficiency

Toru Uchiyama, Satoru Kumaki, Mitsuhiro Fujiwara, Yoshinobu Nishida, Ikuko Hakozaki, Kaori Imai, D. U. Wei, Miyako Yoshinari, Yoji Sasahara, Shigeru Tsuchiya

Research output: Contribution to journalArticle

4 Citations (Scopus)
Original languageEnglish
Pages (from-to)575-578
Number of pages4
JournalPediatrics International
Volume47
Issue number5
DOIs
Publication statusPublished - 2005 Oct 1

Keywords

  • JAK3 japanese
  • Mutation
  • Severe combined immunodeficiency

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Uchiyama, T., Kumaki, S., Fujiwara, M., Nishida, Y., Hakozaki, I., Imai, K., Wei, D. U., Yoshinari, M., Sasahara, Y., & Tsuchiya, S. (2005). A novel JAK3 mutation in a Japanese patient with severe combined immunodeficiency. Pediatrics International, 47(5), 575-578. https://doi.org/10.1111/j.1442-200x.2005.02103.x