Clinical report: A novel VEGFR3 mutation causes milroy disease
- Author
- BUTLER, Matthew G1 ; DAGENAIS, Susan L1 ; ROCKSON, Stanley G2 ; GLOVER, Thomas W1 3
[1] Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, United States
[2] Stanford School of Medicine, Stanford University, Stanford, California, United States
[3] Department of Pediatrics, University of Michigan, Ann Arbor, Michigan, United States - Source
American journal of medical genetics. Part A. 2007, Vol 143, Num 11, pp 1212-1217, 6 p ; ref : 1/2 p
- Publisher
- Wiley-Liss, Hoboken, NJ
- Publication country
- United States
- Document type
- Article
- Language
- English
- Author keyword
- Milroy disease VEGFR3 lymphedema
- Keyword (fr)
- Etude cas Lymphoedème Maladie Mutation Appareil circulatoire pathologie Lymphatique pathologie
- Keyword (en)
- Case study Lymphedema Disease Mutation Cardiovascular disease Lymphatic vessel disease
- Keyword (es)
- Estudio caso Linfedema Enfermedad Mutación Aparato circulatorio patología Linfático patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B12 Cardiology. Vascular system / 002B12B Blood and lymphatic vessels / 002B12B04 Diseases of the lymphatic vessels
- Discipline
- Cardiology. Circulatory system Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18817750
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.31703 
https://dx.doi.org/10.1002/ajmg.a.31703
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