Recurrent p.N767S mutation in the ATP2A2 gene in a Japanese family with haemorrhagic Darier disease clinically mimicking epidermolysis bullosa simplex with mottled pigmentation

T Hamada; S Yasumoto; T Karashima; N Ishi; H Shimada; Y Kawano; S Imayama; J A McGrath; T Hashimoto

doi:10.1111/j.1365-2133.2007.08086.x

Recurrent p.N767S mutation in the ATP2A2 gene in a Japanese family with haemorrhagic Darier disease clinically mimicking epidermolysis bullosa simplex with mottled pigmentation

T Hamada, S Yasumoto, T Karashima, N Ishi, H Shimada, Y Kawano, S Imayama, J A McGrath, T Hashimoto

Dermatology

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

15 Citations (Scopus)

Original language	English
Pages (from-to)	605 - 608
Number of pages	4
Journal	British Journal of Dermatology
Volume	157
Issue number	3
DOIs	https://doi.org/10.1111/j.1365-2133.2007.08086.x
Publication status	Published - Sept 2007

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10.1111/j.1365-2133.2007.08086.x

Cite this

Hamada, T., Yasumoto, S., Karashima, T., Ishi, N., Shimada, H., Kawano, Y., Imayama, S., McGrath, J. A., & Hashimoto, T. (2007). Recurrent p.N767S mutation in the ATP2A2 gene in a Japanese family with haemorrhagic Darier disease clinically mimicking epidermolysis bullosa simplex with mottled pigmentation. British Journal of Dermatology, 157(3), 605 - 608. https://doi.org/10.1111/j.1365-2133.2007.08086.x

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title = "Recurrent p.N767S mutation in the ATP2A2 gene in a Japanese family with haemorrhagic Darier disease clinically mimicking epidermolysis bullosa simplex with mottled pigmentation",

author = "T Hamada and S Yasumoto and T Karashima and N Ishi and H Shimada and Y Kawano and S Imayama and McGrath, {J A} and T Hashimoto",

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Hamada, T, Yasumoto, S, Karashima, T, Ishi, N, Shimada, H, Kawano, Y, Imayama, S, McGrath, JA & Hashimoto, T 2007, 'Recurrent p.N767S mutation in the ATP2A2 gene in a Japanese family with haemorrhagic Darier disease clinically mimicking epidermolysis bullosa simplex with mottled pigmentation', British Journal of Dermatology, vol. 157, no. 3, pp. 605 - 608. https://doi.org/10.1111/j.1365-2133.2007.08086.x

TY - JOUR

T1 - Recurrent p.N767S mutation in the ATP2A2 gene in a Japanese family with haemorrhagic Darier disease clinically mimicking epidermolysis bullosa simplex with mottled pigmentation

AU - Hamada, T

AU - Yasumoto, S

AU - Karashima, T

AU - Ishi, N

AU - Shimada, H

AU - Kawano, Y

AU - Imayama, S

AU - McGrath, J A

AU - Hashimoto, T

PY - 2007/9

Y1 - 2007/9

U2 - 10.1111/j.1365-2133.2007.08086.x

DO - 10.1111/j.1365-2133.2007.08086.x

M3 - Article

SN - 1365-2133

VL - 157

SP - 605

EP - 608

JO - British Journal of Dermatology

JF - British Journal of Dermatology

IS - 3

ER -