Different mutations in PDE4D associated with developmental disorders with mirror phenotypes

Author(s):
Lindstrand, A.; Grigelioniene, G.; Nilsson, D.; Pettersson, M.; Hofmeister, W.; Anderlid, B.M.; Kant, S.G.; Ruivenkamp, C.A.L.; Gustavsson, P.; Valta, H.; Geiberger, S.; Topa, A.; Lagerstedt-Robinson, K.; Taylan, F.; Wincent, J.; Laurell, T.; Pekkinen, M.; Nordenskjold, M.; Makitie, O.; Nordgren, A.
Published
2014
Publication type
Article / Letter to editor
Clinical GeneticsCopy-NumberDevelopmentalOther NeurologyOther Endocrinology
Date issued
2014-01-31
Language
English
Is part of
Journal of Medical Genetics (2014), Vol. 51, no. 1, p. 45-54
hdl
1887/104679
doi
10.1136/jmedgenet-2013-101937