Identification of FOXP1 Deletions in Three Unrelated Patients with Mental Retardation and Significant Speech and Language Deficits

Mental retardation affects 2-3% of the population and shows a high heritability. Neurodevelopmental disorders that include pronounced impairment in language and speech skills occur less frequently. For most cases, the molecular basis of mental retardation with or without speech and language disorder...

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Αποθηκεύτηκε σε:
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Κύριοι συγγραφείς: Horn, Denise, Kapeller, Johannes, Rivera-Brugués, Núria, Moog, Ute, Lorenz-Depiereux, Bettina, Eck, Sebastian, Hempel, Maja, Wagenstaller, Janine, Gawthrope, Alex, Monaco, Anthony P, Bonin, Michael, Riess, Olaf, Wohlleber, Eva, Illig, Thomas, Bezzina, Connie R, Franke, Andre, Spranger, Stephanie, Villavicencio-Lorini, Pablo, Seifert, Wenke, Rosenfeld, Jochen, Klopocki, Eva, Rappold, Gudrun A, Strom, Tim M
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Wiley Subscription Services, Inc., A Wiley Company 2010
Θέματα:
Mutation in Brief
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3049153/
https://ncbi.nlm.nih.gov/pubmed/20848658
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.21362
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