Memory Disorders

CTNND2—a candidate gene for reading problems and mild intellectual disability
Wolfgang Hofmeister, Daniel Nilsson, Alexandra Topa, Britt-Marie Anderlid, Fahimeh Darki, Hans Matsson, Isabel Tapia Páez, Torkel Klingberg, Lena Samuelsson, Valtteri Wirta, Francesco Vezzi, Juha Kere, Magnus Nordenskjöld, Elisabeth Syk Lundberg, Anna Lindstrand

Journal of Medical Genetics Feb 2015, 52 (2) 111-122; DOI: 10.1136/jmedgenet-2014-102757
Correlation between FMR1 expression and clinical phenotype in discordant dichorionic–diamniotic monozygotic twin sisters with the fragile x mutation
Wen Huang, Shiyu Luo, Jianjun Ou, Furong Zhu, Yan Xia, Jinjie Xue, Qian Pan, Lingqian Wu, Ranhui Duan

Journal of Medical Genetics Mar 2014, 51 (3) 159-164; DOI: 10.1136/jmedgenet-2013-101978

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Memory Disorders