Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Killimann, M."'
Autor:
Hendrickx, J., Coucke, P., Bossuyt, P., Wauters, Jan, Raeymaekers, Peter, Marchau, F., Smit, G.P.A., Stolte, I., Sardharwalla, I.B., Berthelot, J., van den Bergh, I., Berger, R., Van Broeckhoven, Christine, Davidson, J., Baussan, C., Wapenaar, M., Killimann, M., Fernandes, J., Willems, P.J.
Publikováno v:
Human molecular genetics
Human molecular genetics, 2(5), 583-589. Oxford University Press
Human Molecular Genetics, 2(5), 583-589. Oxford University Press
Human molecular genetics, 2(5), 583-589. Oxford University Press
Human Molecular Genetics, 2(5), 583-589. Oxford University Press
X-linked phosphorylase kinase (PHK) deficiency causes X-linked liver glycogenosis (XLG) which is the most frequent fiver glycogen storage disorder in man. Recently we assigned XLG to the Xp22 chromosomal region by linkage analysis in two families seg