SOX10 Mutation in Waardenburg Syndrome Type II
- Author
- ISO, Manami1 ; FUKAMI, Maki1 ; HORIKAWA, Reiko2 ; AZUMA, Noriyuki3 ; KAWASHIRO, Nobuko4 ; OGATA, Tsutomu1
[1] Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, Tokyo, Japan
[2] Division of Endocrinology and Metabolism, National Center for Child Health and Development, Tokyo, Japan
[3] Division of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
[4] Division of Otorhinolaryngology, National Center for Child Health and Development, Tokyo, Japan - Source
American journal of medical genetics. Part A. 2008, Vol 146, Num 16, pp 2162-2163, 2 p ; ref : 1/2 p
- Publisher
- Wiley-Liss, Hoboken, NJ
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Mutation Syndrome de Waardenburg Pathologie ORL Pathologie de l'appareil digestif Pathologie de la peau Trouble de la pigmentation
- Keyword (en)
- Mutation Waardenburg syndrome ENT disease Digestive diseases Skin disease Pigmentation disorder
- Keyword (es)
- Mutación Waardenburg síndrome ORL patología Aparato digestivo patología Piel patología Trastorno pigmentación
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B08 Dermatology / 002B08F Pigmentary diseases of the skin
- Discipline
- Dermatology Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 20532035
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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DOI
10.1002/ajmg.a.32403 
https://dx.doi.org/10.1002/ajmg.a.32403
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