Twelve novel FBN1 mutations in Marfan syndrome and Marfan related phenotypes test the feasibility of FBN1 mutation testing in clinical practice.

Detalles Bibliográficos
Autores principales: Halliday, D, Hutchinson, S, Lonie, L, Hurst, J, Firth, H, Handford, P, Wordsworth, P
Formato: Journal article
Lenguaje:English
Publicado: 2002