An integrated approach to management of Marfan syndrome caused by an FBN1 exon 18 mutation in an Australian Aboriginal family

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Autoria(s): Summers, K. M.; Xu, D.; West, J. A.; McGill, J. J.; Galbraith, A.; Whight, C. M.; Brocque, S. L.; Nataatmadja, M.; Kong, L. K.; Dondey, J.; Stark, D.; West, M. J.

Contribuinte(s)	Hayden, M. R.
Data(s)	01/01/2004
Identificador	http://espace.library.uq.edu.au/view/UQ:73198
Idioma(s)	eng
Publicador	Blackwell Munksgaard
Palavras-Chave	#Genetics & Heredity #Dural Ectasia #Gene #Polymorphism #C1 #321011 Medical Genetics #730107 Inherited diseases (incl. gene therapy)
Tipo	Journal Article