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Listar por palabra clave "Type I von Willebrand's disease mutation detection"

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Association of the 3467C>T mutation (T1156M) in the von Willebrands factor gene with dominant type 1 von Willebrands disease

Casaña-Gargallo, María Pilar; Francisco Martínez; Saturnino Haya; Espinós-Armero, Carmen Ángeles; José Antonio Aznar (Springer-Verlag, 2001-07)

[EN] Type I is the most frequent form of von Willebrand's disease, which is characterized by a quantitative partial deficiency of von Willebrand's factor. At present, only two mutations located in the D3 domain (C1149R, ...

Mostrando ítems 1-1 de 1