Citations for
1AGA, AGU
Plasma lysosomal enzyme activities in congenital disorders of glycosylation, galactosemia and fructosemia.
Michelakakis H, Moraitou M, Mavridou I, Dimitriou E.
Clin Chim Acta 401(1-2):81-3. Epub 2008 Dec 3. 2009
2AGA, AGU
Structural basis of aspartylglucosaminuria.
Saito S, Ohno K, Sugawara K, Suzuki T, Togawa T, Sakuraba H.
Biochem Biophys Res Commun 377(4):1168-72. Epub 2008 Nov 4. 2008
3AGA, AGA2, AGA3, AR
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.
Hillmer AM, Hanneken S, Ritzmann S, Becker T, Freudenberg J, Brockschmidt FF, Flaquer A, Freudenberg-Hua Y, Jamra RA, Metzen C, Heyn U, Schweiger N, Betz RC, Blaumeiser B, Hampe J, Schreiber S, Schulze TG, Hennies HC, Schumacher J, Propping P, Ruzicka T, Cichon S, Wienker TF, Kruse R, Nothen MM.
Am J Hum Genet 77(1):140-8. Epub 2005 May 18. 2005
4AGA, AGU
A novel aspartylglucosaminuria mutation affects translocation of aspartylglucosaminidase.
Saarela J, von Schantz C, Peltonen L, Jalanko A.
Hum Mutat 24(4):350-1. 2004
5AGA, AGU
Autoproteolytic activation of human aspartylglucosaminidase.
Saarela J, Oinonen C, Jalanko A, Rouvinen J, Peltonen L.
Biochem J 378(Pt 2):363-71. 2004