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

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

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

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

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

T Hamada,S Yasumoto,T Karashima,N Ishii,H Shimada,Y Kawano,S Imayama,JA McGrath,T Hashimoto,T Hamada,S Yasumoto,T Karashima,N Ishii,H Shimada,Y Kawano,S Imayama,JA McGrath,T Hashimoto,

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

PUBLICATION TYPE: Research Support, Non-U.S. Gov

Journal: The British journal of dermatology

VOLUME: 157

Page Numbers: 605-8

Journal Abbreviation: Br. J. Dermatol.

ISSN: 0007-0963

DAY: 16

MONTH: 07

YEAR: 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. Information

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LANGUAGE: eng

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

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

AFFILIATION: Department of Dermatology, Kurume University School of Medicine, 67 Asahimachi, Kurume 830-0011, Japan. hamataka@med.kurume-u.ac.jp

Country: England

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MEDLINETA: Br J Dermatol

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