Literature citations
De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.
Hamdan F.F.; Daoud H.; Rochefort D.; Piton A.; Gauthier J.; Langlois M.; Foomani G.; Dobrzeniecka S.; Krebs M.O.; Joober R.; Lafreniere R.G.; Lacaille J.C.; Mottron L.; Drapeau P.; Beauchamp M.H.; Phillips M.S.; Fombonne E.; Rouleau G.A.; Michaud J.L.;
Am. J. Hum. Genet. 87:671-678(2010)
Cited for: FUNCTION; INVOLVEMENT IN MRLIAF; VARIANTS ALA-215; MET-445; SER-570 AND ASN-613;
Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.
Vernes S.C.; MacDermot K.D.; Monaco A.P.; Fisher S.E.;
Eur. J. Hum. Genet. 17:1354-1358(2009)
Cited for: VARIANT ALA-215;
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.
Horn D.; Kapeller J.; Rivera-Brugues N.; Moog U.; Lorenz-Depiereux B.; Eck S.; Hempel M.; Wagenstaller J.; Gawthrope A.; Monaco A.P.; Bonin M.; Riess O.; Wohlleber E.; Illig T.; Bezzina C.R.; Franke A.; Spranger S.; Villavicencio-Lorini P.; Seifert W.; Rosenfeld J.; Klopocki E.; Rappold G.A.; Strom T.M.;
Hum. Mutat. 31:E1851-E1860(2010)
Cited for: VARIANTS PRO-5; VAL-101; ALA-215; PRO-261; SER-390 AND SER-570; VARIANT MRLIAF THR-597;
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder.
Sollis E.; Graham S.A.; Vino A.; Froehlich H.; Vreeburg M.; Dimitropoulou D.; Gilissen C.; Pfundt R.; Rappold G.A.; Brunner H.G.; Deriziotis P.; Fisher S.E.;
Hum. Mol. Genet. 25:546-557(2016)
Cited for: VARIANTS MRLIAF GLY-465; CYS-514; ARG-534 AND THR-597; VARIANTS THR-107; ALA-215 AND SER-570; CHARACTERIZATION OF VARIANTS MRLIAF GLY-465; CYS-514; ARG-534 AND THR-597; CHARACTERIZATION OF VARIANTS THR-107; ALA-215 AND SER-570; FUNCTION; SELF-ASSOCIATION; SUBCELLULAR LOCATION; INTERACTION WITH FOXP2;
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