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Netherton syndrome in two japanese siblings with a novel mutation in the SPINK5 gene : immunohistochemical studies of LEKTI and other epidermal molecules

Author
SHIMOMURA, Y1 ; SATO, N1 ; KARIYA, N1 ; TAKATSUKA, S1 ; ITO, M1
[1] Department of Dermatology, Niigata University School of Medicine, Asahimachi-dori, Niigata 951-8510, Japan
Source

British journal of dermatology (1951). 2005, Vol 153, Num 5, pp 1026-1030, 5 p ; ref : 20 ref

CODEN
BJDEAZ
ISSN
0007-0963
Scientific domain
Dermatology
Publisher
Blackwell, Edinburgh / Blackwell, London / Blackwell, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Author keyword
LEKTI Nethenon syndrome SPINK5 compound heterozygous mutations desmoglem 1 elafin
Keyword (fr)
Dermatologie Elafine Epiderme Erythrodermie ichtyosiforme Netherton Etude cas Fratrie Gène Immunohistochimie Mutation Japon Anatomopathologie Dyskératose Hyperkératose Maladie héréditaire Peau pathologie Asie
Keyword (en)
Dermatology Elafin Epidermis Netherton syndrome Case study Sibling Gene Immunohistochemistry Mutation Japan Anatomic pathology Dyskeratosis Hyperkeratosis Genetic disease Skin disease Asia
Keyword (es)
Dermatología Elafina Epidermis Eritrodermia ictiosiforme Netherton Estudio caso Hermandad Gen Inmunohistoquímica Mutación Japón Anatomía patológica Disqueratosis Hiperqueratosis Enfermedad hereditaria Piel patología Asia
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B08 Dermatology / 002B08I Dyskeratosis

Discipline
Dermatology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
17239620

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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