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

doi:10.1007/s004030050175

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

Graduate School of Medicine Dentistry and Pharmaceutical Sciences

Research output: Contribution to journal › Article › peer-review

13 Citations (Scopus)

Original language	English
Pages (from-to)	174-176
Number of pages	3
Journal	Archives of Dermatological Research
Volume	289
Issue number	3
DOIs	https://doi.org/10.1007/s004030050175
Publication status	Published - 1997

Keywords

GB3
Herlitz
JEB
Laminin 5

ASJC Scopus subject areas

Dermatology

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10.1007/s004030050175

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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

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

In: Archives of Dermatological Research, Vol. 289, No. 3, 1997, p. 174-176.

Research output: Contribution to journal › Article › peer-review

Shimizu, H, Takizawa, Y, McGrath, JA, Pulkkinen, L, Christiano, AM, Uitto, J, Burgeson, RE, 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, vol. 289, no. 3, pp. 174-176. https://doi.org/10.1007/s004030050175

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. / Absence of R42X and R635X mutations in the LAMB3 gene in 12 Japanese patients with junctional epidermolysis bullosa. In: Archives of Dermatological Research. 1997 ; Vol. 289, No. 3. pp. 174-176.

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

keywords = "GB3, Herlitz, JEB, Laminin 5",

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

note = "Funding Information: Acknowledgement Supported in part by USPHS, NIH grant POI AR 38923 (JN), and by the Dermatology Foundation (LP).",

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AU - Shimizu, H.

AU - Takizawa, Y.

AU - McGrath, J. A.

AU - Pulkkinen, L.

AU - Christiano, A. M.

AU - Uitto, J.

AU - Burgeson, R. E.

AU - Iwatsuki, K.

AU - Niimi, N.

AU - Noguchi, M.

AU - Imayama, S.

AU - Abe, Y.

AU - Shirakata, Y.

AU - Hagiwara, S.

AU - Saida, T.

AU - Ogawa, H.

AU - Hashimoto, I.

AU - Nishikawa, T.

N1 - Funding Information: Acknowledgement Supported in part by USPHS, NIH grant POI AR 38923 (JN), and by the Dermatology Foundation (LP).

PY - 1997

Y1 - 1997

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KW - Herlitz

KW - JEB

KW - Laminin 5

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

Keywords

ASJC Scopus subject areas

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