CTNND2-a candidate gene for reading problems and mild intellectual disability
Page 1 of 1
CTNND2-a candidate gene for reading problems and mild intellectual disability
Hofmeister W, Nilsson D, Topa A, Anderlid BM, Darki F, Matsson H, Tapia Páez I, Klingberg T, Samuelsson L, Wirta V, Vezzi F, Kere J, Nordenskjöld M, Syk Lundberg E, Lindstrand A. CTNND2-a candidate gene for reading problems and mild intellectual disability. J Med Genet. 2014 Dec 3. pii: jmedgenet-2014-102757. doi: 10.1136/jmedgenet-2014-102757. [Epub ahead of print]
Similar topics
» MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus
» A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGT
» Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy
» Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus
» Impaired Development Of Neural-Crest Cell Derived Organs and Intellectual Disability Caused By MED13L Haploinsufficiency
» A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGT
» Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy
» Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus
» Impaired Development Of Neural-Crest Cell Derived Organs and Intellectual Disability Caused By MED13L Haploinsufficiency
Page 1 of 1
Permissions in this forum:
You cannot reply to topics in this forum