No evidence for coding region mutations in the retinoblastoma-associated Kruppel-associated box protein gene (RBaK) causing familial hyperaldosteronism type II

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Autoria(s): So, Albertina; Jeske, Yvette W.A.; Gordon, Richard D.; Duffy, David; Kelemen, Livia; Stowasser, Michael

Data(s)	01/12/2006
Identificador	http://espace.library.uq.edu.au/view/UQ:82087
Idioma(s)	eng
Publicador	Blackwell Publishing Ltd
Palavras-Chave	#Endocrinology #Hyperaldosteronism type II #RBaK #CX #321004 Endocrinology #730105 Endocrine organs and diseases (incl. diabetes) #1103 Clinical Sciences #110306 Endocrinology
Tipo	Journal Article