Absence of R42X and R635X mutations in the LAMB3 gene in 12 Japanese patients with junctional epidermolysis bullosa

H. Shimizu, Y. Takizawa, J. A. McGrath, L. Pulkkinen, A. M. Christiano, J. Uitto, R. E. Burgeson, K. Iwatsuki, N. Niimi, M. Noguchi, S. Imayama, Y. Abe, Y. Shirakata, S. Hagiwara, T. Saida, H. Ogawa, I. Hashimoto, T. Nishikawa

Research output: Contribution to journalArticle

13 Citations (Scopus)
Original languageEnglish
Pages (from-to)174-176
Number of pages3
JournalArchives of Dermatological Research
Volume289
Issue number3
DOIs
Publication statusPublished - Mar 18 1997

Keywords

  • GB3
  • Herlitz
  • JEB
  • Laminin 5

ASJC Scopus subject areas

  • Dermatology

Cite this

Shimizu, H., Takizawa, Y., McGrath, J. A., Pulkkinen, L., Christiano, A. M., Uitto, J., Burgeson, R. E., Iwatsuki, K., Niimi, N., Noguchi, M., Imayama, S., Abe, Y., Shirakata, Y., Hagiwara, S., Saida, T., Ogawa, H., Hashimoto, I., & Nishikawa, T. (1997). Absence of R42X and R635X mutations in the LAMB3 gene in 12 Japanese patients with junctional epidermolysis bullosa. Archives of Dermatological Research, 289(3), 174-176. https://doi.org/10.1007/s004030050175