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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 23, 2025. (Total: 235602Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Stuttering and FOXP2[original query]
A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering.
Neurobiology of disease 2014 Sep 69 23-31.
Han Tae-Un, Park John, Domingues Carlos F, Moretti-Ferreira Danilo, Paris Emily, Sainz Eduardo, Gutierrez Joanne, Drayna Denn
FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum.
Journal of medical genetics 2016 Aug .
Reuter Miriam S, Riess Angelika, Moog Ute, Briggs Tracy A, Chandler Kate E, Rauch Anita, Stampfer Miriam, Steindl Katharina, Gläser Dieter, Joset Pascal, , Krumbiegel Mandy, Rabe Harald, Schulte-Mattler Uta, Bauer Peter, Beck-Wödl Stefanie, Kohlhase Jürgen, Reis André, Zweier Christia
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