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Article

CTNND2-a candidate gene for reading problems and mild intellectual disability.

Journal of medical genetics - 1 Feb 2015

Hofmeister Wolfgang, Nilsson Daniel, Topa Alexandra, Anderlid Britt-Marie, Darki Fahimeh, Matsson Hans, Tapia Páez Isabel, Klingberg Torkel, Samuelsson Lena, Wirta Valtteri, Vezzi Francesco, Kere Juha, Nordenskjöld Magnus, Syk Lundberg Elisabeth, Lindstrand Anna

Abstract excerpt

BACKGROUND: Cytogenetically visible chromosomal translocations are highly informative as they can pinpoint strong effect genes even in complex genetic disorders. METHODS AND RESULTS: Here, we report a mother and daughter, both with borderline intelligence and learning problems within the dyslexia spectrum, and two apparently balanced reciprocal translocations: t(1;8)(p22;q24) and t(5;18)(p15;q11). By low coverage...

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Identifiers

PMID: 25473103
DOI: 10.1136/jmedgenet-2014-102757

Genes

CTNND2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

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