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Various activating TIE2 tyrosine kinase domain mutations, including the recurrent R849W substitution, cause cutaneomucosal venous malformation (VMCM) in a paradominant fashion

Bibliographic reference Limaye, Nisha ; Wouters, Vinciane ; Uebelhoer, Mélanie ; Irrthum, Alexandre ; Boon, Laurence ; et. al. Various activating TIE2 tyrosine kinase domain mutations, including the recurrent R849W substitution, cause cutaneomucosal venous malformation (VMCM) in a paradominant fashion.57th Annual Meeting of the American Society of Human Genetics (San Diego, USA, du 23/10/2007 au 27/10/2007).
Permanent URL http://hdl.handle.net/2078.1/138022